Fungicidal compositions

ABSTRACT

The present invention provides a composition comprising a combination of components A) and B), wherein component A) is a compound of formula (I) and the component (B) is a further fungicide, insecticide or herbicide.

RELATED APPLICATION INFORMATION

This application is a 371 of International Application No.PCT/CN2012/073665, filed 9 Apr. 2012, which claims priority toInternational Application No. PCT/CN2011/084016, filed 14 Dec. 2011, thecontents of which are incorporated herein by reference.

The present invention relates to novel fungicidal compositions whichcomprise fungicidally active pyridylamidine compounds for the treatmentof phytopathogenic diseases of useful plants, especially phytopathogenicfungi, and to a method of controlling phytopathogenic diseases on usefulplants.

Certain phenylamidine derivatives are described in WO2008/101682 asmicrobicidally active ingredients in pesticides.

The present invention provides a composition comprising a combination ofcomponents A) and B), wherein component A) is a compound of formula (I)

wherein

R₁ and R₂ are each independently selected from hydrogen, C₁-C₄ alkyl,C₃-C₄ alkenyl, C₃-C₄ alkynyl, (R₁₀)carbonyl and (R₁₀)oxycarbonyl;

or R₁ and R₂ together with the nitrogen atom to which they are attachedform a 5- or 6 membered cyclic group which may be saturated orunsaturated and may contain a further heteroatom selected from S or O;

R₃ represents hydrogen, halogen, cyano, nitro, mercapto, hydroxy,—C(═S)NH₂, —SF₅, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, a 5-membered heterocycle containing 1-4 nitrogen atoms,piperidino, morpholino, thiomorpholino, formyl, hydroxycarbonyl, C₂-C₇alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl,C₄-C₇ haloalkenyloxycarbonyl, C₂-C₇ alkylcarbonyl, C₂-C₇haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆haloalkylsulfonyl, C₁-C₆ hydroxyalkyl, phenyl or benzyl wherein thephenyl and benzyl are optionally substituted by one or more groupsindependently selected from the group consisting of halogen, cyano,hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl;

R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄alkyl, C₁-C₄haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, methylamino and dimethylamino;

R₅ is hydrogen, C₁-C₁₂alkyl, C₃-C₁₂alkenyl, C₃-C₁₂alkynyl,C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl orbenzylsulfonyl, or is C₁-C₁₂alkyl, C₂-C₁₂alkenyl, C₂-C₁₂alkynyl,C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl orbenzylsulfonyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, nitro, hydroxy,mercapto, azido, formyl, C₂-C₇alkylcarbonyl, C₂-C₇haloalkylcarbonyl,C₁-C₆alkyl, C₁-C₆haloalkyl, C₁-C₆alkoxy, C₁-C₆haloalkoxy,C₁-C₆alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆alkylsulfonyl; or

R₅ is formyl, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₃-C₁₂alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl,phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂ alkenyloxycarbonyl, C₄-C₁₂alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl orphenoxycarbonyl, or is C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl,C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl,phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂ alkenyloxycarbonyl, C₄-C₁₂alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl orphenoxycarbonyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, C₁-C₆ alkyl, C₁-C₆haloalkyl and C₁-C₆ alkoxy; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-,(R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—,(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkynyl, C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-N—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein thegroup B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—,—ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)₂—,—S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—,—C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, inturn, are mono- to poly-substituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, mercapto,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-,A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-,A-(C₃-C₈cycloalkyl)- or A-O—(C₃-C₈cycloalkyl)-;

wherein A is a three- to ten-membered monocyclic or fused bicyclic ringsystem which can be aromatic, partially saturated or fully saturated andcan contain 1 to 4 hetero atoms selected from the group consisting ofnitrogen, oxygen and sulphur, it not being possible for each ring systemto contain —O—O—, —S—S— and —O—S— fragments, and it being possible forthe three- to ten-membered ring system to be itself mono- orpolysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, azido, formyl, carboxy, ═O,═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl, C₁-C₆haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈ halocycloalkyl,C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy,C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, benzyl, benzyloxy, phenyl andphenoxy, where the benzyl, benzyloxy, phenyl and phenoxy, in turn, maybe mono- to polysubstituted by substituents independently selected fromthe group consisting of halogen, cyano, nitro, hydroxy, mercapto, amino,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

A2) by substituents independently selected form the group consisting of(R₁₄)S(═O)(═NR₁₃)—, (R₁₄)(R₁₅)S(═O)═N—; —Si(R₅₁)(R₅₂)(R₅₃), —NR₅₇R₅₈,—C(═O)NR₅₇R₅₈, C(═S)NR₅₇R₅₈, HC(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)—,(C₁-C₆haloalkyl)C(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)C₁-C₆alkyl-,(C₁-C₆haloalkyl)C(═NOR₅₉)C₁-C₆alkyl-, N(C₁-C₆alkyl)aminosulfonyl andN,N-di(C₁-C₆alkyl)aminosulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl,C₄-C₉ halocycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₂-C₇haloalkoxycarbonyl, C₃-C₇ alkenyloxycarbonyl, C₃-C₇ alkynyloxycarbonyl,C₄-C₉ cycloalkoxycarbonyl, C₂-C₇ alkylthiocarbonyl andbenzyloxycarbonyl, and benzyloxycarbonyl mono- to polysubstituted bysubstituents independently selected from the group consisting ofhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;or

A4) by substituents independently selected from the group consisting ofhydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl,═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionallysubstituted by one or more group selected from the group consisting ofhalogen, methyl, halomethyl; or

R₅ is —N═C(R₈)(R₉); or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, CN, NO₂, OH,SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl,C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R₆ is selected from hydrogen and SH;

R₇ is hydrogen, halogen or C₁-C₄ alkyl;

R₈ and R₉, independently from each other, are hydrogen, halogen, cyano,C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, formyl,C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, carboxy, C₂-C₁₂alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonyl, or C₁-C₁₂ alkyl, C₂-C₁₂alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂alkenylcarbonyl, C₂-C₁₂ alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonylmono- to polysubstituted by substituents independently selected from thegroup consisting of halogen, cyano, nitro, hydroxy, mercapto, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or R₈ and R₉ together froma C₂-C₈ alkylene bridge which may optionally be mono- to polysubstitutedby substituents independently selected from the group consisting ofhalogen, cyano, C₁-C₆ alkyl and C₁-C₆ haloalkyl; or R₈ and R₉,independently from each other, are the groups A-, A-O— orA-(C₁-C₆alkyl)-;

R₁₀ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl or C₁-C₄ haloalkyl;

R₁₃ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl,phenyl and benzyl, or is phenyl and benzyl mono- to polysubstituted byhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy;

R₁₄ and R₁₅, independently of each other, are C₁-C₆ alkyl, C₃-C₈cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzyl or phenylindependently of each other, substituted by substituents selected fromthe group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆haloalkyl and C₁-C₆ alkoxy;

R₅₁, R₅₂, R₆₃, independently of each other, are halogen, cyano, C₁-C₆alkyl, C₂-C₆alkenyl, C₃-C₈ cycloalkyl, C₅-C₈ cycloalkenyl, C₂-C₆alkynyl, C₁-C₆ alkoxy, benzyl or phenyl;

R₅₄, R₅₅, R₆₆, independently of each other, are C₁-C₆ alkyl, C₃-C₆alkenyl, C₃-C₈ cycloalkyl, C₃-C₆ alkynyl, benzyl or phenyl;

R₅₇ and R₆₈, independently of each other, are hydrogen, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈cycloalkyl, C₃-C₈ halocycloalkyl, phenyl or benzyl, where phenyl orbenzyl for their part may be mono- to polysubstituted on the phenyl ringby substituents independently selected from the group consisting ofhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy,or R₅₇ and R₅₈ together with their interconnecting nitrogen atom areaziridino, azetidino, pyrazolino, pyrazolidino, pyrrolino, pyrrolidino,imidazolino, imidazolidino, triazolino, tetrazolino, piperazino,piperidino, morpholino, thiomorpholino, each of which, in turn, may bemono- or polysubstituted by substituents selected from the groupconsisting of methyl, halogen, cyano;

R₅₉ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl,benzyl and phenyl, and benzyl and phenyl mono- to polysubstituted byhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy;

R₆₀ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, benzylor phenyl, or benzyl or phenyl mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, cyano,hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;

R₆₂ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈halocycloalkyl, C₃-C₆ alkenyl, C₃-C₆ alkynyl, benzyl or phenyl, orbenzyl or phenyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, C₁-C₆alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl;

and agronomically acceptable salts/metallic complexes/metalloidiccomplexes/isomers/structuralisomers/stereo-isomers/diastereoisomers/enantiomers/tautomers/N-oxidesof those compounds;

and

component B) is a strobilurin fungicide, a sterol biosynthesis inhibitorfungicide, a triazole fungicide, or a pro-triazole fungicide, or a DMIfungicide, or a SDHI fungicide, or a compound selected from the groupconsisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid,Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectinbenzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone,Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos,Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl,Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron,Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione,Bicyclopyrone, Tembotrione, Sulcotrione, Sulcotrione, Auxins,Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl,Methyl-Jasmonate, Cis-Jasmone, Manganese, Cyflufenamid, Tebufloquin andCopper.

A further aspect of present invention provides a composition comprisinga combination of components A) and B) in a synergistically effectiveratio between the component A) and component B).

A further aspect of the present invention provides a method ofcontrolling phytopathogenic diseases on useful plants or on propagationmaterial thereof, which comprises applying to the useful plants, thelocus thereof or propagation material thereof a combination ofcomponents A) and B) in as synergistically effective amount and ratiobetween the component A) and component B).

A further aspect of the present invention relates to novel compoundsaccording to formula (I).

A further aspect of the present invention relates to novel intermediatesto provide compounds according to formula (I).

Preferably, component B is a strobilurin fungicide, a sterolbiosynthesis inhibitor fungicide, a triazole fungicide, a pro-triazolefungicide, a DMI fungicide, a SDHI fungicide, or is a compound selectedfrom Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid, Mefenoxam,Orocymedone, Fluazinam, Procymedone, Carbendazim, Abamectin,Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin,Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos,Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl,Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron,Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione,Bicyclopyrone, Tembotrione, Sulcotrione, Auxins, Trinexapac-ethyl,Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate,Cis-Jasmone, Manganese and Copper.

Preferably, component B is a strobilurin fungicide, a sterolbiosynthesis inhibitor fungicide, a triazole fungicide, a pro-triazolefungicide, a DMI fungicide, a SDHI fungicide, or is a compound selectedfrom the group consisting of Chlorothalonil, Fludioxonil, Cyprodinil,Mandipropamid, Mefenoxam, Orocymedone, Fluazinam, Carbendazim,Thiamethoxam, Glyphosate, 2,4-D, Trinexapac-ethyl, Prohexadione-Ca,Paclobutrazol and cis-Jasmone.

In one group of mixtures, component B is a strobilurin fungicide.

In another group of mixtures, component B is a Sterol biosynthesisinhibitor

In another group of mixtures, component B is a triazole fungicide or aprotriazole compound.

In another group of mixtures, component B is a DMI fungicide.

In another group of mixtures, component B is a SDHI fungicide.

In another group of mixtures, component B is a compound of formula (III)

wherein R^(70′) is phenyl, which is unsubstituted or substituted with 1,2 or 3 substituents selected from halogen, haloalkyl, haloalkoxy andcyano, and;

R^(71′) is phenyl, which is unsubstituted or substituted with 1, 2 or 3substituents selected from halogen, haloalkyl, haloalkoxy and cyano.

Preferred compounds of formula (III) are(S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanoland3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol.

In another group of mixtures, component B is selected from the groupconsisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid,Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectinbenzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone,Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos,Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl,Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron,Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione,Bicyclopyrone, Tembotrione, Sulcotrione, Auxins (e.g. 2,4-D and MCPA),Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol, Acibenzolar-S-methyl,Methyl-Jasmonate, Cis-Jasmone, Manganese and Copper, preferably from thegroup consisting of Chlorothalonil, Fludioxonil, Cyprodinil,Fenpropidin, Mandipropamid, Mefenoxam, Orocymedone, Fluazinam,Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectin benzoate,Imidacloprid, Tefluthrin, Thiamethoxam, Lambda-cyhalothrin,Gamma-cyhalothrin, Profenofos, Lufenuron, Diflubenzuron, Cypermethrin,Novaluron, Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan,Betacyfluthrin, Triflumuron, Teflubenzuron, SulcotrioneAcephat,Glyphosate, Glufosinate, Mesotrione, Bicyclopyrone, Tembotrione,Sulcotrione, Auxins, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol,Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese andCopper, more preferably from the group consisting of Chlorothalonil,Fludioxonil, Cyprodinil, Fenpropidin, Mandipropamid, Mefenoxam,Orocymedone, Fluazinam, Carbendazim, Thiamethoxam, Glyphosate, 2,4-D,Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol and cis-Jasmone.

In a preferred embodiment the component B) is a compound selected fromChlorothalonil, Fludioxonil, Cyprodinil, Fenpropidin, Mandipropamid,Fenpropimorph, Fluazinam, Procymedone, Carbendazim, Abamectin,Clothianidin, Emamectin benzoate, Imidacloprid, Tefluthrin, Mefenoxam,Orocymedone, Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin,Profenofos, Lufenuron, Diflubenzuron, Cypermethrin, Novaluron,Bifenthrin, Methomyl, Chlopyrifos, Methamidophos, Endosulfan,Betacyfluthrin, Triflumuron, Teflubenzuron, Acephat, Glyphosate,Glufosinate, Mesotrione, Bicyclopyrone, Tembotrione, Sulcotrione, 2,4-D,MCPA, Trinexapac-ethyl, Prohexadione-Ca, Paclobutrazol,Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone, Manganese, Copper,Coumoxystrobin, Dicloaminostrobin, Flufenoxystrobin, Pyrametostrobin,Pyraoxystrobin, Trifloxystrobin, Azoxystrobin, Pyraclostrobin,Picoxystrobin, Jiaxiangjunzhi, Enoxastrobin, Triclopyricarb, thecompound of formula II, Cyproconazole, Difenoconazole, Metconazole,Propiconazole, Epoxiconazole, Tebuconazole, Flutriafol, Ipconazole,prothioconazole,(S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol,3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol,Pyrisoxazole,3-(Difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamide,N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide,Isopyrazam, Sedaxane, Boscalid, Fluxapyroxad, Penthiopyrad, Penflufen,Bixafen and Fluopyram.

The term strobilurin fungicide is well known to the person skilled inthe art, and includes, for example, Coumoxystrobin, Dicloaminostrobin,Flufenoxystrobin, Pyrametostrobin, Pyraoxystrobin, Trifloxystrobin,Azoxystrobin, Pyraclostrobin, Picoxystrobin, Jiaxiangjunzhi,Enoxastrobin, Triclopyricarb, Fluoxastrobin, Dimoxystrobin,Fenaminostrobin and the compound of formula (II). Preferred strobilurinfungicides are Azoxystrobin, Pyraclostrobin and Picoxystrobin. Even morepreferred strobilurin fungicides are Azoxystrobin and Pyraclostrobin.

The term sterol biosynthesis inhibitor fungicide is well known to theperson skilled in the art, and includes, for example, Spiroxamine,Fenpropimorph, Tridemorph, Fenpropidin, Fenhexamid, Terbinafine,Naftifine

The term triazole fungicide is well known to the person skilled in theart, and includes, for example, Cyproconazole, Difenoconazole,Metconazole, Propiconazole, Epoxiconazole, Tebuconazole, Flutriafol,Ipconazole and1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol[CAS number 120983-64-4]. Preferred triazole fungicide compounds areCyproconazole, Difenoconazole, Metconazole and Tebuconazole. Even morepreferred is Cyproconazole.

The term pro-triazole fungicide is well known to the person skilled inthe art and includes, for example, prothioconazole.

The term DMI fungicides is well known to the person skilled in the artand includes, for example,(S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol,3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)isoxazol-4-yl]-pyridin-3-yl-methanoland Pyrisoxazole. Preferred DMI fungicides are(S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanoland3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol.

The term SDHI fungicide is well known to the person skilled in the artand includes, for example,N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide,Isopyrazam, Sedaxane, Boscalid Fluxapyroxad, Penthiopyrad, Penflufen,Bixafen, Fluopyram,3-(Difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamide,Preferred SDHI fungicides areN-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide,Isopyrazam,3-(Difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamideand Fluxapyroxad.

The term Auxins is well known to the person skilled in the art andincludes, for example, 2,4-D, MCPA and Dicamba

In a further preferred embodiment the component B is Chlorothalonil. Ina further preferred embodiment the component B is Fludioxonil. In afurther preferred embodiment the component B is Cyprodinil. In a furtherpreferred embodiment the component B is Fenpropidin. In a furtherpreferred embodiment the component B is Mandipropamid. In a furtherpreferred embodiment the component B is Fluazinam. In a furtherpreferred embodiment the component B is Procymedone. In a furtherpreferred embodiment the component B is Carbendazim. In a furtherpreferred embodiment the component B is Abamectin. In a furtherpreferred embodiment the component B is Clothianidin. In a furtherpreferred embodiment the component B is Emamectin benzoate. In a furtherpreferred embodiment the component B is Imidacloprid. In a furtherpreferred embodiment the component B is Tefluthrin. In a furtherpreferred embodiment the component B is Mefenoxam. In a furtherpreferred embodiment the component B is Orocymedone. In a furtherpreferred embodiment the component B is Thiamethoxam. In a furtherpreferred embodiment the component B is Lambda-cyhalothrin. In a furtherpreferred embodiment the component B is Gamma-cyhalothrin. In a furtherpreferred embodiment the component B is Profenofos. In a furtherpreferred embodiment the component B is Lufenuron. In a furtherpreferred embodiment the component B is Diflubenzuron. In a furtherpreferred embodiment the component B is Cypermethrin. In a furtherpreferred embodiment the component B is Novaluron. In a furtherpreferred embodiment the component B is Bifenthrin. In a furtherpreferred embodiment the component B is Methomyl. In a further preferredembodiment the component B is Chlopyrifos. In a further preferredembodiment the component B is Methamidophos. In a further preferredembodiment the component B is Endosulfan. In a further preferredembodiment the component B is Betacyfluthrin. In a further preferredembodiment the component B is Triflumuron. In a further preferredembodiment the component B is Teflubenzuron. In a further preferredembodiment the component B is Acephat. In a further preferred embodimentthe component B is Glyphosate. In a further preferred embodiment thecomponent B is Glufosinate. In a further preferred embodiment thecomponent B is Mesotrione. In a further preferred embodiment thecomponent B is Bicyclopyrone. In a further preferred embodiment thecomponent B is Tembotrione. In a further preferred embodiment thecomponent B is Sulcotrione. In a further preferred embodiment thecomponent B is 2,4-D. In a further preferred embodiment the component Bis MCPA. In a further preferred embodiment the component B isTrinexapac-ethyl. In a further preferred embodiment the component B isProhexadione-Ca. In a further preferred embodiment the component B isPaclobutrazol. In a further preferred embodiment the component B isAcibenzolar-5-methyl. In a further preferred embodiment the component Bis Methyl-Jasmonate. In a further preferred embodiment the component Bis Cis-Jasmone. In a further preferred embodiment the component B isManganese. In a further preferred embodiment the component B is Copper.In a further preferred embodiment the component B is Cyflufenamid. In afurther preferred embodiment the component B is Tebufloquin. In afurther preferred embodiment the component B is Coumoxystrobin. In afurther preferred embodiment the component B is Dicloaminostrobin. In afurther preferred embodiment the component B is Flufenoxystrobin. In afurther preferred embodiment the component B is Pyrametostrobin. In afurther preferred embodiment the component B is Pyraoxystrobin. In afurther preferred embodiment the component B is Trifloxystrobin. In afurther preferred embodiment the component B is Azoxystrobin. In afurther preferred embodiment the component B is Pyraclostrobin. In afurther preferred embodiment the component B is Picoxystrobin. In afurther preferred embodiment the component B is Jiaxiangjunzhi. In afurther preferred embodiment the component B is Enoxastrobin. In afurther preferred embodiment the component B is Triclopyricarb. In afurther preferred embodiment the component B is Fluoxastrobin. In afurther preferred embodiment the component B is Dimoxystrobin. In afurther preferred embodiment the component B is Fenaminostrobin In afurther preferred embodiment the component B is the compound of formulaII. In a further preferred embodiment the component B is Cyproconazole.In a further preferred embodiment the component B is Difenoconazole. Ina further preferred embodiment the component B is Metconazole. In afurther preferred embodiment the component B is Propiconazole. In afurther preferred embodiment the component B is Epoxiconazole. In afurther preferred embodiment the component B is Tebuconazole. In afurther preferred embodiment the component B is Flutriafol. In a furtherpreferred embodiment the component B is Ipconazole. In a furtherpreferred embodiment the component B is1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol[CAS number 120983-64-4]. In a further preferred embodiment thecomponent B is prothioconazole. In a further preferred embodiment thecomponent B is(S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)isoxazol-4-yl]-pyridin-3-yl-methanol.In a further preferred embodiment the component B is3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol.In a further preferred embodiment the component B is Pyrisoxazole. In afurther preferred embodiment the component B is3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-Pyrazole-4-carboxamide.In a further preferred embodiment the component B isN-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide.In a further preferred embodiment the component B is Isopyrazam. In afurther preferred embodiment the component B is Sedaxane. In a furtherpreferred embodiment the component B is Boscalid, In a further preferredembodiment the component B is Fluxapyroxad. In a further preferredembodiment the component B is Penthiopyrad. In a further preferredembodiment the component B is Penflufen. In a further preferredembodiment the component B is Bixafen. In a further preferred embodimentthe component B is Fluopyram. In a further preferred embodiment thecomponent B is1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol.

The active ingredient mixture according to the invention may bring aboutthe additive enhancement of the spectrum of action with respect to thephytopathogen to be controlled that may in principle be expected butachieves a synergistic effect which extends the range of action of thecomponent (A) and of the component (B) in two ways. Firstly, the ratesof application of the component (A) and of the component (B) may belowered whilst the action remains equally good. Secondly, the activeingredient mixture may still achieve a high degree of phytopathogencontrol even where the two individual components have become totallyineffective in such a low application rate range. This allows, on theone hand, a substantial broadening of the spectrum of phytopathogensthat can be controlled and, on the other hand, increased safety in use.

However, besides the actual synergistic action with respect tofungicidal activity, the pesticidal compositions according to theinvention may also have further surprising advantageous properties whichcan also be described, in a wider sense, as synergistic activity.Examples of such advantageous properties that may be mentioned are: abroadening of the spectrum of fungicidal activity to otherphytopathogens, for example to resistant strains; a reduction in therate of application of the active ingredients; synergistic activityagainst animal pests, such as insects or representatives of the orderAcarina; a broadening of the spectrum of pesticidal activity to otheranimal pests, for example to resistant animal pests; adequate pestcontrol with the aid of the compositions according to the invention,even at a rate of application at which the individual compounds aretotally ineffective; advantageous behaviour during formulation and/orupon application, for example upon grinding, sieving, emulsifying,dissolving or dispensing; increased storage stability; improvedstability to light; more advantageous degradability; improvedtoxicological and/or ecotoxicological behaviour; improvedcharacteristics of the useful plants including: emergence, crop yields,more developed root system, tillering increase, increase in plantheight, bigger leaf blade, less dead basal leaves, stronger tillers,greener leaf colour, less fertilizers needed, less seeds needed, moreproductive tillers, earlier flowering, early grain maturity, less plantverse (lodging), increased shoot growth, improved plant vigor, and earlygermination; or any other advantages familiar to a person skilled in theart.

Substituents at a nitrogen atom are always different from halogen. Ahydroxy, mercapto or amino substituent is not to be placed on anα-carbon relative to a heteroatom of a core fragment.

The alkyl groups occurring in the definitions of the substituents can bestraight-chain or branched and are, for example, methyl, ethyl,n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl,hexyl, heptyl and octyl and their branched isomers. Alkoxy, alkenyl andalkynyl radicals are derived from the alkyl radicals mentioned. Thealkenyl and alkynyl groups can be mono- or polyunsaturated.

The cycloalkyl groups occurring in the definitions of the substituentsare, for example, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.

Halogen is generally fluorine, chlorine, bromine or iodine, preferablyfluorine, bromine or chlorine. This also applies, correspondingly, tohalogen in combination with other meanings, such as haloalkyl orhaloalkoxy.

Haloalkyl groups preferably have a chain length of from 1 to 6 carbonatoms. Haloalkyl is, for example, fluoromethyl, difluoromethyl,trifluoromethyl, chloromethyl, dichloromethyl, trichloromethyl,2,2,2-trifluoroethyl, 2-fluoroethyl, 2-chloroethyl, pentafluoroethyl,1,1-difluoro-2,2,2-trichloroethyl, 2,2,3,3-tetrafluoroethyl,2,2,2-trichloroethyl, 5,5,5-trifluoropentan-1-yl,5,5-difluoro-pentan-1-yl, 6,6,6-trifluorohexan-1-yl,6,6-difluoro-hexan-1-yl, heptafluoro-prop-2-yl and 2-fluoro-prop-2-yl;preferably trichloromethyl, difluorochloromethyl, difluoromethyl,trifluoromethyl and dichlorofluoromethyl.

Suitable haloalkenyl groups are alkenyl groups which are mono- di- ortrisubstituted by halogen, halogen being fluorine, chlorine, bromine andiodine and in particular fluorine and chlorine, for example2,2-difluoro-1-methylvinyl, 3-fluoropropenyl, 3-chloropropenyl,3-bromopropenyl, 2,3,3-trifluoropropenyl, 2,3,3-trichloropropenyl and4,4,4-trifluorobut-2-en-1-yl.

Suitable haloalkynyl groups are, for example, alkynyl groups which aremono- or polysubstituted by halogen, halogen being bromine, iodine andin particular fluorine and chlorine, for example 3-fluoropropynyl,3-chloropropynyl, 3-bromopropynyl, 3,3,3-trifluoropropynyl and4,4,4-trifluorobut-2-yn-1-yl.

Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy,isobutoxy, sec-butoxy and tert-butoxy; preferably methoxy and ethoxy.Halogenalkoxy is, for example, fluoromethoxy, difluoromethoxy,trifluoromethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy,2-fluoroethoxy, 2-chloroethoxy, 2,2-difluoroethoxy and2,2,2-trichloroethoxy; preferably difluoromethoxy, 2-chloroethoxy andtrifluoromethoxy.

Alkoxycarbonyl is, for example, methoxycarbonyl, ethoxycarbonyl,propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl,isobutoxycarbonyl, sec-butoxycarbonyl or tert-butoxycarbonyl; preferablymethoxycarbonyl or ethoxycarbonyl. Haloalkoxy groups preferably have achain length of from 1 to 6 carbon atoms. Haloalkoxy is, for example,fluoromethoxy, difluoromethoxy, trifluoromethoxy, 2,2,2-trifluoroethoxy,1,1,2,2-tetrafluoroethoxy, 2-fluoroethoxy, 2-chloroethoxy,2,2-difluoroethoxy and 2,2,2-trichloroethoxy; preferablydifluoromethoxy, 2-chloroethoxy and trifluoromethoxy. Alkylthio groupspreferably have a chain length of from 1 to 6 carbon atoms.

Alkoxyalkyl is, for example, methoxymethyl, methoxyethyl, ethoxymethyl,ethoxyethyl, n-propoxymethyl, n-propoxyethyl, isopropoxymethyl orisopropoxyethyl.

Alkylthio is, for example, methylthio, ethylthio, propylthio,isopropylthio, n-butylthio, isobutylthio, sec-butylthio ortert-butylthio, preferably methylthio and ethylthio. Alkylsulfinyl is,for example, methylsulfinyl, ethylsulfinyl, propylsulfinyl,isopropylsulfinyl, n-butylsulfinyl, isobutylsulfinyl, sec-butylsulfinyl,tert-butylsulfinyl; preferably methylsulfinyl and ethylsulfinyl.Alkylsulfonyl is, for example, methylsulfonyl, ethylsulfonyl,propylsulfonyl, isopropylsulfonyl, n-butylsulfonyl, isobutylsulfonyl,sec-butylsulfonyl or tert-butylsulfonyl; preferably methylsulfonyl orethylsulfonyl.

C₂-C₆ alkylcarbonyl is, for example, methylcarbonyl, ethylcarbonyl,propylcarbonyl, isopropylcarbonyl, n-butylcarbonyl, isobutylcarbonyl,sec-butylcarbonyl, tert-butylcarbonyl or n-pentylcarbonyl and theirbranched isomers, preferably methylcarbonyl and ethylcarbonyl.Haloalkylcarbonyl radicals are derived from the alkyl radicalsmentioned.

In the context of the present invention “mono- to polysubstituted” inthe definition of the substituents, means typically, depending on thechemical structure of the substituents, monosubstituted to seven-timessubstituted, preferably monosubstituted to five-times substituted, morepreferably mono-, double- or triple-substituted.

According to the present invention, a three- to ten-membered monocyclicor fused bicyclic ring system which may be aromatic, partially saturatedor fully saturated is, depending of the number of ring members, forexample, selected from the group consisting of

cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, where saidcycloalkylgroups for their part may be preferably unsubstituted orsubstituted by C₁-C₆alkyl or halogen, or is phenyl, benzyl, naphthyl orthe following heterocyclic groups: pyrrolyl; pyridyl; pyrazolyl;pyrimidyl; pyrazinyl; imidazolyl; thiadiazolyl; quinazolinyl; furyl;oxadiazolyl; indolizinyl; pyranyl; isobenzofuranyl; thienyl;naphthyridinyl; (1-methyl-1H-pyrazol-3-yl)-; (1-ethyl-1H-pyrazol-3-yl)-;(1-propyl-1H-pyrazol-3-yl)-; (1H-pyrazol-3-yl)-;(1,5-dimethyl-1H-pyrazol-3-yl)-; (4-chloro-1-methyl-1H-pyrazol-3-yl)-;(1H-pyrazol-1-yl)-; (3-methyl-1H-pyrazol-1-yl)-;(3,5-dimethyl-1H-pyrazol-1-yl)-; (3-isoxazolyl)-;(5-methyl-3-isoxazolyl)-; (3-methyl-5-isoxazolyl)-; (5-isoxazolyl)-;(1H-pyrrol-2-yl)-; (1-methyl-1H-pyrrol-2-yl)-; (1H-pyrrol-1-yl)-;(1-methyl-1H-pyrrol-3-yl)-; (2-furanyl)-; (5-methyl-2-furanyl)-;(3-furanyl)-; (5-methyl-2-thienyl)-; (2-thienyl)-; (3-thienyl)-;(1-methyl-1H-imidazol-2-yl)-; (1H-imidazol-2-yl)-;(1-methyl-1H-imidazol-4-yl)-; (1-methyl-1H-imidazol-5-yl)-;(4-methyl-2-oxazolyl)-; (5-methyl-2-oxazolyl)-; (2-oxazolyl)-;(2-methyl-5-oxazolyl)-; (2-methyl-4-oxazolyl)-; (4-methyl-2-thiazolyl)-;(5-methyl-2-thiazolyl)-; (2-thiazolyl)-; (2-methyl-5-thiazolyl)-;(2-methyl-4-thiazolyl)-; (3-methyl-4-isothiazolyl)-;(3-methyl-5-isothiazolyl)-; (5-methyl-3-isothiazolyl)-;(1-methyl-1H-1,2,3-triazol-4-yl)-; (2-methyl-2H-1,2,3-triazol-4-yl)-;(4-methyl-2H-1,2,3-triazol-2-yl)-; (1-methyl-1H-1,2,4-triazol-3-yl)-;(1,5-dimethyl-1H-1,2,4-triazol-3-yl)-;(3-methyl-1H-1,2,4-triazol-1-yl)-; (5-methyl-1H-1,2,4-triazol-1-yl)-;(4,5-dimethyl-4H-1,2,4-triazol-3-yl)-;(4-methyl-4H-1,2,4-triazol-3-yl)-; (4H-1,2,4-triazol-4-yl)-;(5-methyl-1,2,3-oxadiazol-4-yl)-; (1,2,3-oxadiazol-4-yl)-;(3-methyl-1,2,4-oxadiazol-5-yl)-; (5-methyl-1,2,4-oxadiazol-3-yl)-;(4-methyl-3-furazanyl)-; (3-furazanyl)-;(5-methyl-1,2,4-oxadiazol-2-yl)-; (5-methyl-1,2,3-thiadiazol-4-yl)-;(1,2,3-thiadiazol-4-yl)-; (3-methyl-1,2,4-thiadiazol-5-yl)-;(5-methyl-1,2,4-thiadiazol-3-yl)-; (4-methyl-1,2,5-thiadiazol-3-yl)-;(5-methyl-1,3,4-thiadiazol-2-yl)-; (1-methyl-1H-tetrazol-5-yl)-;(1H-tetrazol-5-yl)-; (5-methyl-1H-tetrazol-1-yl)-;(2-methyl-2H-tetrazol-5-yl)-; (2-ethyl-2H-tetrazol-5-yl)-;(5-methyl-2H-tetrazol-2-yl)-; (2H-tetrazol-2-yl)-; (2-pyridyl)-;(6-methyl-2-pyridyl)-; (4-pyridyl)-; (3-pyridyl)-;(6-methyl-3-pyridazinyl)-; (5-methyl-3-pyridazinyl)-; (3-pyridazinyl)-;(4,6-dimethyl-2-pyrimidinyl)-; (4-methyl-2-pyrimidinyl)-;(2-pyrimidinyl)-; (2-methyl-4-pyrimidinyl)-; (2-chloro-4-pyrimidinyl)-;(2,6-dimethyl-4-pyrimidinyl)-; (4-pyrimidinyl)-;(2-methyl-5-pyrimidinyl)-; (6-methyl-2-pyrazinyl)-; (2-pyrazinyl)-;(4,6-dimethyl-1,3,5-triazin-2-yl)-; (4,6-dichloro-1,3,5-triazin-2-yl)-;(1,3,5-triazin-2-yl)-; (4-methyl-1,3,5-triazin-2-yl)-;(3-methyl-1,2,4-triazin-5-yl)-; (3-methyl-1,2,4-triazin-6-yl)-;

wherein each R₂₆ is methyl, each R₂₇ and each R₂₈ are independentlyhydrogen, C₁-C₃alkyl, C₁-C₃alkoxy, C₁-C₃alkylthio or trifluoromethyl, X₄is oxygen or sulfur and r=1, 2, 3 or 4.

There no free valency is indicated in those definitions, for example asin

the linkage site is located at the carbon atom labelled “CH” or in acase such as, for example,

at the bonding site indicated at the bottom left.

The following substituents definitions, including preferred definitions,may be combined in any combination:

R₁ and R₂ are each independently selected from hydrogen, C₁-C₄ alkyl,C₃-C₄ alkenyl, C₃-C₄ alkynyl, (R₁₀)carbonyl and (R₁₀)oxycarbonyl;

or R₁ and R₂ together with the nitrogen atom to which they are attachedform a 5- or 6 membered cyclic group which may be saturated orunsaturated and may contain a further heteroatom selected from S or O.

Preferably, R₁ and R₂ are each independently selected from hydrogen,C₁-C₄ alkyl, C₃-C₄ alkenyl and C₃-C₄ alkynyl;

or R₁ and R₂ together with the nitrogen atom to which they are attachedform a pyrrolidine or piperidine.

More preferably, R₁ and R₂ are each independently selected from hydrogenor C₁-C₄ alkyl;

or R₁ and R₂ together with the nitrogen atom to which they are attachedform a pyrrolidine or piperidine.

Even more preferably, R₁ and R₂ are each independently selected fromhydrogen or C₁-C₄ alkyl.

More preferably again, R₁ and R₂ are each C₁-C₄ alkyl.

More favourably again, R₁ and R₂ are each independently selected frommethyl, ethyl and isopropyl.

Yet more favourably, R₁ is methyl and R₂ is selected from methyl, ethyland isopropyl.

Yet more favourably still, R₁ is methyl and R₂ is selected from ethyland isopropyl.

Most preferably, R₁ is methyl and R₂ is ethyl.

R₃ represents hydrogen, halogen, cyano, nitro, mercapto, hydroxy,—C(═S)NH₂, —SF₅, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino,di(C₁-C₆alkyl)amino, a 5-membered heterocycle containing 1-4 nitrogenatoms, piperidino, morpholino, thiomorpholino, formyl, hydroxycarbonyl,C₂-C₇alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl,C₄-C₇ haloalkenyloxycarbonyl, C₂-C₇ alkylcarbonyl, C₂-C₇haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆haloalkylsulfonyl, C₁-C₆ hydroxyalkyl, phenyl or benzyl wherein thephenyl and benzyl are optionally substituted by one or more groupsindependently selected from the group consisting of halogen, cyano,hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl.

Preferably, R₃ represents hydrogen, halogen, cyano, mercapto, hydroxy,C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ haloalkenyl, C₂-C₄alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino,tetrazolino, formyl, C₂-C₅ alkylcarbonyl, C₂-C₅ haloalkylcarbonyl,C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆alkylsulfonyl, C₁-C₆haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆ haloalkylsulfonyl or C₁-C₆hydroxyalkyl.

More preferably, R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆cycloalkyl, amino, C₁-C₂alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino,imidazolino, triazolino, formyl, phenyl, C₂-C₄ alkylcarbonyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl or C₁-C₆hydroxyalkyl.

Even more preferably, R₃ represents hydrogen, halogen, cyano, C₁-C₄alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl,amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino,triazolino, formyl, C₂-C₄alkylcarbonyl, C₁-C₄alkylthio, C₁-C₄alkylsulfinyl, C₁-C₄ alkylsulfonyl, C₁-C₄ haloalkylthio, C₁-C₄haloalkylsulfinyl or C₁-C₄ haloalkylsulfonyl or C₁-C₆ hydroxyalkyl.

More preferably again, R₃ represents hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,C₃-C₆ cycloalkyl, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl or C₁-C₄alkylsulfonyl.

Favourably, R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl,C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl or C₁-C₄ alkylsulfonyl.

Even more favourably, R₃ represents hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy or C₃-C₆ cycloalkyl.

More favourably again, R₃ represents hydrogen, halogen, C₁-C₄ alkyl,C₁-C₄ haloalkyl, cyclopropyl, ethynyl or C₁-C₄ alkoxy.

Yet more favourably, R₃ is selected from hydrogen, bromine, iodine,methyl, CHF₂, cyclopropyl, ethynyl and methoxy.

Yet more favourably still, R₃ represents hydrogen, bromine, iodine,methyl, difluoromethyl or methoxy.

Most preferably, R₃ represents bromine or methyl.

R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, methylamino or dimethylamino.

Preferably, R₄ is selected from hydrogen, fluorine, chlorine, bromine,C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₃-C₆cycloalkyl.

More preferably, R₄ is selected from fluorine, chlorine, bromine, C₁-C₄alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₃-C₆cycloalkyl.

Even more preferably, R₄ is selected from fluorine, chlorine, methyl,ethyl, ethenyl, propyl, propenyl, isopropyl, isopropenyl, cyclopropanyl,methoxy, ethoxy, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoromethyl.

More preferably again, R₄ is selected from methyl, ethyl, methoxy,fluorine and chlorine.

More favourably again, R₄ is selected from methyl, methoxy, fluorine andchlorine.

Most preferably, R₄ is methyl.

In another group of compounds, R₄ is selected from methoxy, fluorine andchlorine.

R₅ is hydrogen, C₁-C₁₂alkyl, C₃-C₁₂alkenyl, C₃-C₁₂alkynyl,C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl orbenzylsulfonyl, or is C₁-C₁₂alkyl, C₂-C₁₂alkenyl, C₂-C₁₂alkynyl,C₁-C₁₂alkylsulfonyl, C₂-C₁₂alkenylsulfonyl, phenylsulfonyl orbenzylsulfonyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, nitro, hydroxy,mercapto, azido, formyl, C₂-C₇alkylcarbonyl, C₂-C₇haloalkylcarbonyl,C₁-C₆alkyl, C₁-C₆haloalkyl, C₁-C₆alkoxy, C₁-C₆haloalkoxy,C₁-C₆alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆alkylsulfonyl; or

R₅ is formyl, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₃-C₁₂alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl,phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂alkenyloxycarbonyl, C₄-C₁₂alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl orphenoxycarbonyl, or is C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl,C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl, benzylcarbonyl,phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂ alkenyloxycarbonyl, C₄-C₁₂alkynyloxycarbonyl, C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl orphenoxycarbonyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, C₁-C₆ alkyl, C₁-C₆haloalkyl and C₁-C₆ alkoxy; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-,(R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—,(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein thegroup B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—,—ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)₂—,—S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—,—C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, inturn, are mono- to poly-substituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, mercapto,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-,A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-,A-(C₃-C₈cycloalkyl)- or A-O—(C₃-C₈cycloalkyl)-; or

wherein A is a three- to ten-membered monocyclic or fused bicyclic ringsystem which can be aromatic, partially saturated or fully saturated andcan contain 1 to 4 hetero atoms selected from the group consisting ofnitrogen, oxygen and sulphur, it not being possible for each ring systemto contain —O—O—, —S—S— and —O—S— fragments, and it being possible forthe three- to ten-membered ring system to be itself mono- orpolysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, nitro, azido, formyl, carboxy,═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl,C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, benzyl,benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy, phenyl andphenoxy, in turn, may be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, cyano,nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl; or

A2) by substituents independently selected form the group consisting of(R₁₄)S(═O)(═NR₁₃)—, (R₁₄)(R₁₅)S(═O)═N—; —Si(R₅₁)(R₅₂)(R₅₃), —NR₅₇R₅₈,—C(═O)NR₅₇R₅₈, C(═S)NR₅₇R₅₈, HC(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)—,(C₁-C₆haloalkyl)C(═NOR₅₉)—, (C₁-C₆alkyl)C(═NOR₅₉)C₁-C₆alkyl-,(C₁-C₆haloalkyl)C(═NOR₅₉)C₁-C₆alkyl-, N(C₁-C₆alkyl)aminosulfonyl andN,N-di(C₁-C₆alkyl)aminosulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl,C₄-C₉ halocycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₂-C₇haloalkoxycarbonyl, C₃-C₇ alkenyloxycarbonyl, C₃-C₇ alkynyloxycarbonyl,C₄-C₉ cycloalkoxycarbonyl, C₂-C₇ alkylthiocarbonyl andbenzyloxycarbonyl, and benzyloxycarbonyl mono- to polysubstituted bysubstituents independently selected from the group consisting ofhalogen, cyano, hydroxy, C₁-C₆alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;or

A4) by substituents independently selected from the group consisting ofhydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl,═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionallysubstituted by one or more group selected from the group consisting ofhalogen, methyl, halomethyl; or

R₅ is —N═C(R₈)(R₉); or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O, S or Natoms, wherein there are no adjacent O atoms, which is optionallysubstituted by one or more groups independently selected from halogen,CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl,C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂.

Preferably, R₅ represents hydrogen, C₁-C₁₂ alkylsulfonyl, C₁-C₁₂ alkyl,C₃-C₁₂ alkenyl, C₃-C₁₂ alkynyl, or is C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl,C₂-C₁₂ alkynyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, nitro, hydroxy,mercapto, azido, formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₆₁)(R₆₂)(R₆₃)Si—(C₁-C₁₂alkyl)-,(R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—,(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or

R₅ is C₁-C₆alkyl-B—C₁-C₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein thegroup B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—,—ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)₂—,—S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—,—C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, inturn, are mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, mercapto,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is selected from A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-,A-(C₃-C₆alkenyl)-, A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-,A-O—(C₄-C₆alkynyl)-, A-(C₃-C₈cycloalkyl)- and A-O—(C₃-C₈cycloalkyl)-;

wherein A is a three- to ten-membered monocyclic or fused bicyclic ringsystem which can be aromatic, partially saturated or fully saturated andcan contain 1 to 4 hetero atoms selected from the group consisting ofnitrogen, oxygen and sulphur, it not being possible for each ring systemto contain —O—O—, —S—S— and —O—S— fragments, and it being possible forthe three- to ten-membered ring system to be itself mono- orpolysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, nitro, azido, formyl, carboxy,═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl,C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, C₃-C₈halocycloalkyloxy, C₃-C₈ cycloalkenyloxy, C₃-C₈ halocycloalkenyloxy,benzyl, benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy,phenyl and phenoxy, in turn, may be mono- to polysubstituted bysubstituents independently selected from the group consisting ofhalogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl,C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇alkynyloxycarbonyl, C₄-C₉ cycloalkoxycarbonyl and benzyloxycarbonyl, andbenzyloxycarbonyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, C₁-C₆alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or

A4) by substituents independently selected from the group consisting ofhydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl,═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionallysubstituted by one or more group selected from the group consisting ofhalogen, methyl, halomethyl; or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O, S or Natoms, wherein there are no adjacent O atoms, which is optionallysubstituted by one or more groups independently selected from halogen,CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₂-C₇alkylcarbonyl, C₂-C₇alkoxycarbonyl,C₄-C₇-alkenyloxycarbonyl, C₄-C₇alkynyloxycarbonyl, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂.

More preferably, R₅ is selected from G¹, G², G³-G⁴, G⁵, G⁶-G⁷, G⁸, G⁹,G¹⁰-G¹¹, G¹², G¹³, G¹⁴, G¹⁵ and G¹⁶.

More preferably again, R₅ is selected from G¹, G², G⁵, G⁶-G⁸, G⁹,G¹⁰-G¹¹, G¹², G¹⁴, G¹⁵ and G¹⁶.

More favourably again, R₅ is selected from G², G⁵, G⁶-G⁷, G⁸, G⁹,G¹⁰-G¹¹, G¹⁴, G¹⁶.

Most preferably, R₅ is selected from G², G⁵, G⁸ and G¹⁰-G¹¹.

R₆ is selected from hydrogen and SH.

Most preferably, R₆ is hydrogen.

In one group of compounds, R₆ is SH.

R₇ is hydrogen, halogen or C₁-C₄ alkyl.

Preferably, R₇ is hydrogen or C₁-C₄ alkyl.

Most preferably, R₇ is hydrogen.

R₈ and R₉, independently from each other, are hydrogen, halogen, cyano,C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, formyl,C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, carboxy, C₂-C₁₂alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonyl, or C₁-C₁₂ alkyl, C₂-C₁₂alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂alkenylcarbonyl, C₂-C₁₂ alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonylmono- to polysubstituted by substituents independently selected from thegroup consisting of halogen, cyano, nitro, hydroxy, mercapto, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or R₈ and R₉ together froma C₂-C₈ alkylene bridge which may optionally be mono- to polysubstitutedby substituents independently selected from the group consisting ofhalogen, cyano, C₁-C₆ alkyl and C₁-C₆ haloalkyl; or R₈ and R₉,independently from each other, are the groups A-, A-O— orA-(C₁-C₆alkyl)-.

R₁₀ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl or C₁-C₄ haloalkyl.

R₁₃ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl,phenyl and benzyl, or is phenyl and benzyl mono- to polysubstituted byhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy.

R₁₄ and R₁₅, independently of each other, are C₁-C₆ alkyl, C₃-C₈cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzyl or phenylindependently of each other, substituted by substituents selected fromthe group consisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆haloalkyl and C₁-C₆ alkoxy.

R₅₁, R₅₂, R₅₃, independently of each other, are halogen, cyano, C₁-C₆alkyl, C₂-C₆alkenyl, C₃-C₈ cycloalkyl, C₅-C₈ cycloalkenyl, C₂-C₆alkynyl, C₁-C₆ alkoxy, benzyl or phenyl.

R₅₄, R₅₅, R₅₆, independently of each other, are C₁-C₆ alkyl, C₃-C₆alkenyl, C₃-C₈ cycloalkyl, C₃-C₆ alkynyl, benzyl or phenyl.

R₅₇ and R₅₈, independently of each other, are hydrogen, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈cycloalkyl, C₃-C₈ halocycloalkyl, phenyl or benzyl, where phenyl orbenzyl for their part may be mono- to polysubstituted on the phenyl ringby substituents independently selected from the group consisting ofhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy,or R₅₇ and R₅₈ together with their interconnecting nitrogen atom areaziridino, azetidino, pyrazolino, pyrazolidino, pyrrolino, pyrrolidino,imidazolino, imidazolidino, triazolino, tetrazolino, piperazino,piperidino, morpholino, thiomorpholino, each of which, in turn, may bemono- or polysubstituted by substituents selected from the groupconsisting of methyl, halogen, cyano.

R₅₉ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈ halocycloalkyl,benzyl and phenyl, and benzyl and phenyl mono- to polysubstituted byhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl or C₁-C₆ alkoxy.

R₆₀ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, benzylor phenyl, or benzyl or phenyl mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, cyano,hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;

R₆₂ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈halocycloalkyl, C₃-C₆ alkenyl, C₃-C₆ alkynyl, benzyl or phenyl, orbenzyl or phenyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, C₁-C₆alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy.

G¹ is a C₈-C₁₀ fused bicyclic ring system which may be saturated orcomprise one carbon-carbon double bond and is optionally substituted byone or more groups independently selected from hydroxyl, C₁-C₄ alkyl,C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl and cyano.

More preferably, G¹ is a C₉-C₁₀ fused bicyclic ring system which may besaturated or comprise one carbon-carbon double bond and is optionallysubstituted by one or more groups independently selected from hydroxyl,C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl and cyano.

More preferably again, G¹ is a C₉-C₁₀ fused bicyclic ring system whichmay be saturated or comprise one carbon-carbon double bond and isoptionally substituted by one or more groups independently selected fromC₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl.

More favourably, G¹ is a saturated C₉-C₁₀ fused bicyclic ring systemwhich is optionally substituted by one or more groups independentlyselected from C₁-C₄ alkyl, fluoro, methoxy and C₁-C₄ fluoroalkyl.

More favourably again, G¹ is a saturated C₁₀ fused bicyclic ring systemwhich is optionally substituted by one or more groups independentlyselected from C₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl.

Most preferably, G¹ is a saturated C₁₀ fused bicyclic ring system.

G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or moregroups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH,tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl,sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

More preferably again, G² is C₃-C₆ cycloalkenyl, which is optionallysubstituted by one or more groups independently selected from halogen,ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl,n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃,—CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio.

Favourably, G² is C₅-C₆ cycloalkenyl, which is optionally substituted byone or more groups independently selected from halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl and C₁-C₆ alkoxy.

More favourably, G² is a C₅-C₆ cycloalkenyl group optionally substitutedby one or more groups independently selected from fluorine, ethyl,n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl.

More favourably again, G² is a C₅-C₆ cycloalkenyl group optionallysubstituted by one or more fluorine atoms.

Most preferably, G² is a C₅-C₆ cycloalkenyl group.

In one group of compounds, G² is a C₅-C₆ cycloalkenyl group optionallysubstituted one or more groups selected from ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl and C₁-C₆ alkoxy.

Preferably in this group of compounds, G² is a C₅-C₆ cycloalkenyl groupoptionally substituted one or more groups selected from ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl.

G³ is phenyl, which is optionally substituted by one or more groupsindependently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, whereinthe alkyl groups are optionally substituted by one or more halogen.

More preferably again, G³ is phenyl, which is optionally substituted byone or more groups independently selected from hydroxyl, C₁-C₄ alkyl,C₁-C₄ fluoroalkyl, C₁-C₄ alkoxy and halogen.

More favourably again, G³ is phenyl, which is optionally substituted byone or more groups independently selected from hydroxyl, C₁-C₄ alkyl,CHF₂, CF₃, C₁-C₄ alkoxy and halogen.

Yet more favourably, G³ is phenyl, which is optionally substituted byone or more groups independently selected from C₁-C₄ alkyl, CHF₂, CF₃,C₁-C₄ alkoxy and halogen.

Most preferably, G³ is phenyl.

G⁴ is C₃-C₁₂ cycloalkyl which is optionally substituted by one or moregroups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl,C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groupsare optionally substituted by one or more halogen.

More preferably again, G⁴ is C₅-C₆ cycloalkyl which is optionallysubstituted by one or more groups independently selected from hydroxyl,C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen andcyano, wherein the alkyl groups are optionally substituted by one ormore halogen.

More favourably again, G⁴ is C₅-C₆ cycloalkyl which is optionallysubstituted by one or more groups independently selected from hydroxyl,C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy and halogen.

Yet more favourably, G⁴ is C₅-C₆ cycloalkyl which is optionallysubstituted by one or more groups independently selected from C₁-C₄alkyl, C₁-C₄ alkoxy and halogen.

Yet more favourably still, G⁴ is cyclohexyl or cyclopentyl.

Most preferably, G⁴ is cyclohexyl.

G⁵ is C₃-C₇ cycloalkyl, which is optionally substituted by one or moregroups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH,tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl,sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆-alkenyloxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl,C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, phenoxy, —C(═O)NH₂,—C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂.

More preferably, G⁵ is C₃-C₇ cycloalkyl, which is optionally substitutedby one or more groups independently selected from halogen, ethyl,n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl,n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃,—CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆haloalkyl, C₁-C₆ alkoxy, C₃-C₄-alkenyloxy, phenoxy and C₁-C₆ alkylthio.

More preferably again, G⁵ is C₃-C₇ cycloalkyl, which is substituted byone or more groups independently selected from ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy,C₃-C₄-alkenyloxy, phenoxy and C₁-C₆ alkylthio.

More preferably still, G⁵ is C₅-C₇ cycloalkyl, which is substituted byone or more groups independently selected from ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₄ alkoxy, C₃-C₄-alkenyloxy,phenoxy and C₂-C₆ haloalkyl.

More favourably again, G⁵ is C₅-C₆ cycloalkyl, which is substituted byone or more groups independently selected from ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂ and C₂-C₆ haloalkyl.

Yet more favourably, G⁵ is C₅-C₆ cycloalkyl, which is substituted by oneor more groups independently selected from ethyl, n-propyl, iso-propyl,n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂—CH(CH₃)—CH(CH₃)₂, CHF₂ and CF₃.

Most preferably, G⁵ is C₆ cycloalkyl, which is substituted by one ormore groups independently selected from ethyl, n-propyl, iso-propyl,n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂ and —CH(CH₃)—CH(CH₃)₂.

In another group of compounds, G⁵ is a C₅-C₆ cycloalkyl, which isoptionally substituted by one or more halogen.

More preferably in this group, G⁵ is a C₅-C₆ cycloalkyl, which isoptionally substituted by one or more fluorine.

Even more preferably in this group, G⁵ is an unsubstituted C₅-C₆cycloalkyl.

In another group of compounds, G⁵ is a C₅-C₆ cycloalkyl, which isoptionally substituted by one or more groups selected from the groupconsisting of C₁-C₄ alkoxy, C₃-C₄-alkenyloxy or phenoxy.

Preferably in this group of compounds, G⁵ is a C₅-C₆ cycloalkyl, whichis optionally substituted by one or more groups selected from the groupconsisting of methoxy, ethoxy, C₃-C₄ alkenyloxy and phenoxy.

G⁶ is phenyl, which must be substituted by at least one fluorine and isoptionally further substituted by one or more groups independentlyselected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃),C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃),SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio,C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably again, G⁶ is phenyl, which must be substituted by atleast one fluorine and is optionally further substituted by one or moregroups independently selected from halogen, CN, NO₂, OH, SH, CHO,C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆alkynyloxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl.

Yet more preferably, G⁶ is phenyl, which must be substituted by at leastone fluorine and is optionally further substituted by one or more groupsindependently selected from halogen, CN, C₁-C₆ alkyl, C₁-C₆ haloalkyl,C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₃-C₆alkenyloxy, C₃-C₆ alkynyloxy and C₁-C₆ alkylthio.

Favourably, G⁶ is phenyl, which must be substituted by at least onefluorine and is optionally further substituted by one or more groupsindependently selected from halogen, CN, C₁-C₆ alkyl, C₁-C₆ haloalkyland C₁-C₆ alkoxy.

More favourably again, G⁶ is phenyl, which must be substituted by atleast one fluorine and is optionally further substituted by one or moregroups independently selected from halogen, CN, C₁-C₄ alkyl, C₁-C₄haloalkyl and C₁-C₄ alkoxy.

Yet more favourably, G⁶ is phenyl, which must be substituted by at leastone fluorine and is optionally further substituted by one or morehalogen, CHF₂, CF₃ and C₁-C₄ alkyl.

Most preferably, G⁶ is phenyl, which must be substituted by at least onefluorine and is optionally further substituted by one or more methyl,bromine, iodine or chlorine.

In one group of compounds, G⁶ is phenyl substituted at the para-positionby fluorine and further substituted as in the above paragraphs.

In one group of compounds, G⁶ is phenyl substituted at theortho-position by fluorine and further substituted as in the aboveparagraphs.

In one group of compounds, G⁶ is phenyl substituted at the meta-positionby fluorine and further substituted as in the above paragraphs.

G⁷ is methylene.

G⁸ is

G⁹ is

G¹⁰ is phenyl, which is optionally substituted by one or more groupsindependently selected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆haloalkylsulfonyl, phenyl, 2-phenyl-ethynyl and 2-phenyl-ethyl.

Preferably, G¹⁰ is phenyl, which is optionally substituted by one ormore groups independently selected from halogen, CN, NO₂, OH, SH, CHO,C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, phenyl, C₁-C₆alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably, G¹⁰ is phenyl, which is optionally substituted by oneor more groups independently selected from halogen, CN, OH, SH, CHO,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, phenyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl.

More preferably again, G¹⁰ is phenyl, which is optionally substituted byone or more groups independently selected from halogen, CN, OH, SH, CHO,methyl, ethyl, n-propyl, iso-propyl, phenyl, CH₂F, CHF₂, CF₃, CHF—CH₃,CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃),C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH,methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃,SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃

More favourably again, G¹⁰ is phenyl, which is optionally substituted byone or more groups independently selected from halogen, CN, OH, methyl,ethyl, n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃,CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂,C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, phenyl, ethoxy,iso-propyloxy and OCHF₂.

Yet more favourably, G¹⁰ is phenyl, which is optionally substituted byone or more groups independently selected from halogen, CN, methyl,ethyl, n-propyl, iso-propyl, ethenyl, methoxy, ethoxy, iso-propyloxy,phenyl, CHF₂, CF₃, CHF—CH₃ and OCHF₂.

Most preferably, G¹⁰ is phenyl, which is optionally substituted by oneor more groups independently selected from halogen, CN, methyl, ethyl,n-propyl, iso-propyl, ethenyl, methoxy, phenyl, CHF₂, CF₃ and CHF—CH₃.

G¹¹ is methylene substituted by at least one group independentlyselected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄haloalkoxy.

More preferably again, G¹¹ is methylene substituted by at least onegroup independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy and C₁-C₄ haloalkoxy.

More favourably again, G¹¹ is methylene substituted by at least onegroup independently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄alkoxy.

Yet more favourably, G¹¹ is methylene substituted by at least one groupindependently selected from methyl, ethyl, CHF₂ and CF₃.

More favourably still, G¹¹ is methylene substituted by at least onegroup independently selected from methyl, CF₃ and ethyl.

Most preferably, G¹¹ is methylene substituted by at least one groupindependently selected from methyl and ethyl.

G¹² is

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, CN, NO₂, OH,SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl,C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl,C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O,—C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂.

More preferably again, G¹³ is a C₈-C₁₁ spirobicyclic system containing0, 1 or 2 O or N atoms, wherein there are no adjacent O atoms, which isoptionally substituted by one or more groups independently selected fromhalogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and═O.

Most preferably, G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or2 O or N atoms, wherein there are no adjacent O atoms, which isoptionally substituted by one or more groups independently selected fromhalogen, C₁-C₄ alkyl, C₁-C₄ alkoxy and ═O.

G¹⁴ is

G¹⁵ is

G¹⁶ is

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 to 4 members selected from the group consisting ofN, N(R^(69′)), O and S (for example, pyridine, pyrimidine, furan,pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazoleor tetrazole), it not being possible for each ring system to contain—O—O—, —S—S— and —O—S-fragments, and it being possible for the five- tosix-membered ring system to be itself mono- or polysubstituted by groupsselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy,C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl.

More favourably again, G¹⁷ is a five- to six-membered monocyclicheteroaromatic ring system which can contain 1 to 4 members selectedfrom the group consisting of N, N(R^(69′)), O and S, it not beingpossible for each ring system to contain —O—O—, —S—S— and —O—S—fragments, and it being possible for the five- to six-membered-memberedring system to be itself mono- or polysubstituted by groups selectedfrom the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl orbenzyl are optionally substituted by halogen, CN, C₁-C₄ alkyl or C₁-C₄haloalkyl.

Yet more favourably, G¹⁷ is a five- to six-membered monocyclicheteroaromatic ring system which can contain 1 or 2 members selectedfrom the group consisting of N, N(R^(69′)), O and S, it not beingpossible for each ring system to contain —O—O—, —S—S— and —O—S—fragments, and it being possible for the five- to six-membered ringsystem to be itself mono- or polysubstituted by groups selected from thegroup consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl or benzylare optionally substituted by halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl.

Most preferably, G¹⁷ is a five- to six-membered monocyclicheteroaromatic ring system which can contain 1 or 2 members selectedfrom the group consisting of N, O and S, it not being possible for eachring system to contain —O—O—, —S—S— and —O—S— fragments, and it beingpossible for the five- to six-membered ring system to be itself mono- orpolysubstituted by groups selected from the group consisting of halogen,CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenylor fluorophenyl. In one group of compounds, G¹⁷ is selected frompyridine, pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole,imidazole, oxadiazole, thiadiazole or tetrazole each of which may besubstituted by one or more groups selected from the group consisting ofhalogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More favourably again in this group, G¹⁷ is selected from pyridine,pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, imidazole,oxadiazole, thiadiazole or tetrazole each of which may be substituted byone or more groups selected from the group consisting of halogen, CN,C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl orbenzyl, wherein the phenyl or benzyl are optionally substituted byhalogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl.

Yet more favourably in this group, G¹⁷ is selected from pyridine,pyrimidine, furan, pyrrole, thiazole, oxazole, pyrazole, or imidazoleeach of which may be substituted by one or more groups selected from thegroup consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, phenyl or benzyl, wherein the phenyl or benzylare optionally substituted by halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl.

Most preferably in this group, G¹⁷ is selected from pyridine, furan,pyrrole, thiazole or oxazole or imidazole each of which may besubstituted by one or more groups selected from the group consisting ofhalogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄haloalkoxy, phenyl or fluorophenyl.

In another group of compounds, G¹⁷ is a five- to six-membered monocyclicheteroaromatic ring system which can contain 1 member selected from thegroup consisting of N and O (for example, pyridine, furan or pyrrole),it being possible for the five- to six-membered ring system to be itselfmono- or polysubstituted by groups selected from the group consisting ofhalogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy or C₁-C₄haloalkoxy.

Preferably in this group, G¹⁷ is pyridine, furan or pyrrole each ofwhich may be mono- or polysubstituted by groups selected from the groupconsisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy orC₁-C₄ haloalkoxy.

In another group of compounds, G¹⁷ is a five- to six-membered monocyclicheteroaromatic ring system which can contain 2 members selected from thegroup consisting of N, O and S, (for example oxazole or thiazole) it notbeing possible for each ring system to contain —O—O—, —S—S— and —O—S—fragments, and it being possible for the five- to six-membered ringsystem to be itself mono- or polysubstituted by groups selected from thegroup consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl.

Preferably in this group, G¹⁷ is oxazole or thiazole each of which maybe mono- or polysubstituted by groups selected from the group consistingof halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄haloalkoxy, phenyl or fluorophenyl.

R^(1′) is selected from the group consisting of hydrogen, fluorine,C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of eachother, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio.

More preferably again, R^(1′) is selected from the group consisting ofhydrogen, fluorine, C₁-C₄ alkyl and C₁-C₄ fluoroalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of eachother, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio.

Yet more preferably, R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) areselected, independently of each other, from the group consisting ofhydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃,methoxy, ethoxy and S—CH₃ S—CH₂CH₃.

More favourably again, R^(1′) is selected from the group consisting ofhydrogen, fluorine, methyl, CH₂F and CF₃;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of eachother, from the group consisting of hydrogen, fluorine, methyl, CH₂F,CF₃ and methoxy.

Most preferably, R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachhydrogen.

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently ofeach other, from the group consisting of hydrogen, halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, phenyl,C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably again, R^(11′), R^(12′), R^(13′) and R^(14′) areselected, independently of each other, from the group consisting ofhydrogen, cyano, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio.

More favourably again, R^(11′), R^(12′), R^(13′) and R^(14′) areselected, independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, CHF₂, CF₃ and C₁-C₄ alkoxy.

Most preferably, R^(11′), R^(12′), R^(13′) and R^(14′) are selected,independently of each other, from the group consisting of hydrogen,halogen, cyano, C₁-C₄ alkyl and C₁-C₄ alkoxy.

R^(15′) and R^(16′) are independently selected from the group consistingof hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄alkylthio.

More preferably again, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are independently selected from the groupconsisting of hydrogen, halogen, methyl, ethyl, isopropyl, CH₂F, CHF₂,CF₃, CHF—CH₃, CF₂—CH₃ and CF₂CF₃;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄alkylthio.

Favourably, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′),R^(21′) and R^(22′) are independently selected from the group consistingof hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃,CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄alkylthio.

More favourably, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′),R^(21′) and R^(22′) are each independently selected from hydrogen,fluorine, methyl, ethyl, CH₂F, CHF₂ and CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄alkylthio.

More favourably again, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each independently selected fromhydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, methyl, fluorine, chlorine, bromine, ethyl,CH₂F, CHF₂ and CF₃ and isopropyl.

Yet more favourably, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each independently selected fromhydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are each independently selected fromhydrogen, fluorine, chlorine, bromine, methyl, ethyl and isopropyl.

Most preferably, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′),R^(21′), R^(22′), R^(23′), R^(24′) and R^(25′) are each independentlyselected from hydrogen, methyl, ethyl and isopropyl.

In one group of compounds, R^(15′) and R^(16′) are each independentlyselected from the group consisting of hydrogen, methyl, F and CF₃

In this group, R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′),R^(21′) and R^(22′) are most preferably each hydrogen.

In another preferred group of compounds, R^(15′) is as described aboveand R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areeach hydrogen.

In another group of compounds, R^(23′), R^(24′) and R^(25′) areindependently selected from the group consisting of hydrogen, fluorine,chlorine, bromine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃,CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃.

R^(26′) is C(R^(36′))₂, N—O—C₁-C₄-alkyl, N—O—C₂-C₄-alkenyl, N—O—C₂-C₄alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl,N—O-phenyl, N—O-halophenyl, O wherein the N—O-benzyl and N—O-phenyl maybe substituted by one or more groups independently selected from thegroup consisting of halogen, methyl and halomethyl.

Most preferably, R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl,N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl,N—O-benzyl, N—O-phenyl, N—O-halophenyl, O or C(R^(36′)).

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′)and R^(35′) are each independently selected from the group consisting ofhydrogen, hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl andphenyl;

or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond.

More preferably again, R^(27′), R^(28′), R^(29′), R^(30′), R^(31′),R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selectedfrom the group consisting of hydrogen, hydroxyl, C₁-C₄ alkyl, C₁-C₄alkoxy and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond.

More favourably again, R^(27′), R^(28′), R^(29′), R^(30′), R^(31′),R^(32′), R^(33′), R^(34′) and R^(35′) are each independently selectedfrom the group consisting of hydrogen, C₁-C₄ alkyl and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond.

Yet more favourably R^(27′), R^(28′), R^(29′), R^(30′), R^(31′),R^(32′), R^(33′), R^(34′) and R^(35′) are each hydrogen or methyl;

or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond.

Most preferably R^(27′) is hydrogen or methyl;

R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) andR^(35′) are each hydrogen; or R^(28′) and R^(29′) together with the twocarbon atoms to which they are attached form a double bond.

Each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl.

R^(37′) and R^(38′) are selected independently of each other from thegroup consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio.

More preferably again, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom a group consisting of hydrogen, halogen, methyl, ethyl, isopropyl,monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl.

Favourably, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′),R^(43′) and R^(44′) are selected independently of each other from agroup consisting of hydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F,CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂, and CH₂—CF₃.

More favourably again, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are independently selected from the groupconsisting of hydrogen, fluorine, methyl and trifluoromethyl.

Yet more favourably, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are hydrogen or methyl.

Most preferably, R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′),R^(43′) and R^(44′) are hydrogen.

In one group of compounds, R^(38′), R^(39′), R^(40′), R^(41′), R^(42′),R^(43′) and R^(44′) are each hydrogen, and R^(37′) is as defined above.

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl.

More preferably again, R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′)are independently selected from the group consisting of hydrogen,fluorine, chlorine, bromine, iodine, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃,—CF₂—CH₃, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy,methlythio, methylsulfinyl and methylsulfonyl.

Most preferably, R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) areindependently selected from the group consisting of hydrogen, fluorine,chlorine, methyl, CF₃, CHF₂, CH₂F, methoxy, difluoromethoxy andtrifluoromethoxy.

R^(50′) is selected from the group consisting of hydrogen, fluorine,C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected,independently of each other, from the group consisting of hydrogen,fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄alkylthio.

More preferably again, R^(50′), is selected from the group consisting ofhydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected,independently of each other, from the group consisting of hydrogen,fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄haloalkoxy.

Favourably, R^(50′), R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) andR^(56′) are selected, independently of each other, from the groupconsisting of hydrogen, fluorine, methyl, ethyl, CH₂F, CHF₂, CF₃,CHF—CH₃ and CF₂—CH₃.

More favourably again, R^(50′), R^(51′), R^(52′), R^(53′), R^(54′),R^(55′) and R^(56′) are selected, independently of each other, from thegroup consisting of hydrogen, fluorine, methyl, CH₂F and CF₃.

Most preferably, R^(50′), R^(51′), R^(52′), R^(53′), R^(54′), R^(55′)and R^(56′) are each hydrogen.

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently ofeach other, from the group consisting of hydrogen, halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxy, C₂-C₆ haloalkoxy, phenyl,C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen.

More preferably again, R^(57′), R^(58′), R^(59′) and R^(60′) areselected, independently of each other, from the group consisting ofhydrogen, cyano, halogen, C₁-C₆ alkyl and C₁-C₆ haloalkyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen.

More favourably again, R^(57′), R^(58′), R^(59′) and R^(60′) areselected, independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, CHF₂ and CF₃;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen.

Most preferably, R^(57′), R^(58′), R^(59′) and R^(60′) are selected,independently of each other, from the group consisting of hydrogen andhalogen;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen.

In another group of compounds, R^(57′), R^(58′), R^(59′) and R^(60′) areselected, independently of each other, from the group consisting ofhydrogen, phenyl and halophenyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen.

In another group of compounds, R^(57′), R^(58′), R^(59′) and R^(60′) areselected, independently of each other, from the group consisting ofhydrogen, methy, ethyl and hydroxy-C₂-C₄-alkyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen.

Preferably in this group, R^(57′), R^(58′), R^(59′) and R^(60′) areselected, independently of each other, from the group consisting ofhydrogen and hydroxyethyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen.

R^(61′) and R^(62′) are selected independently of each other from thegroup consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄haloalkyl;

R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio.

More preferably again, R^(61′) and R^(62′) are selected independently ofeach other from the group consisting of hydrogen, fluorine, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selectedindependently of each other from the group consisting of hydrogen,fluorine, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄haloalkoxy.

More favourably again, R^(61′) and R^(62′) are selected independently ofeach other from the group consisting of hydrogen, fluorine, methyl,ethyl, CHF₂ and CF₃;

R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) areselected independently of each of there from the group consisting ofhydrogen, fluorine, methyl, ethyl, methoxy, difluoromethoxy,trifluoromethoxy, CHF₂ and CF₃.

Yet more favourably, R^(61′), R^(62′), R^(63′), R^(64′), R^(65′),R^(66′), R^(67′) and R^(68′) are hydrogen, CHF₂, CF₃ or methyl.

Yet more favourably still, R^(61′), R^(62′), R^(63′), R^(64′), R^(65′),R^(66′), R^(67′) and R^(68′) are hydrogen or methyl.

Most preferably, R^(61′), R^(62′), R^(63′), R^(64′), R^(65′), R^(66′),R^(67′) and R^(68′) are hydrogen.

R^(69′) is selected from hydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl and C₁-C₄alkylcarboxy.

More preferably again, R^(69′) is selected from hydrogen, C₁-C₄ alkyland C₁-C₄ alkylcarboxy.

More favourably again, R^(69′) is selected from hydrogen and C₁-C₄alkyl.

Most preferably, R^(69′) is hydrogen.

n is 0 or 1.

In one preferred group of compounds, n is 0.

In another preferred group of compounds, n is 1.

p and q are independently selected from 0 and 1.

In one group of compounds, p and q are 0.

In another group of compounds, p and q are 1

In another group of compounds, p is 1 and q is 0.

r, s and t are independently selected from 0 and 1.

More preferably again, r and s are 0 and t is 1 or 0.

Most preferably, r, s and t are each 0.

In a group of compounds of formula I, R₁ and R₂ are each independentlyselected from hydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl and C₃-C₄ alkynyl;

or R₁ and R₂ together with the nitrogen atom to which they are attachedform a pyrrolidine or piperidine;

R₃ represents hydrogen, halogen, cyano, mercapto, hydroxy, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ haloalkenyl, C₂-C₄ alkynyl, C₁-C₄alkoxy, C₁-C₄ haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino,di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino, triazolino, tetrazolino,formyl, C₂-C₅ alkylcarbonyl, C₂-C₅ haloalkylcarbonyl, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆haloalkylsulfinyl, C₁-C₆ haloalkylsulfonyl or C₁-C₆ hydroxyalkyl;

R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄alkylsulfonyl, methylamino and dimethylamino;

R₅ represents hydrogen, C₁-C₁₂-alkylsulfonyl, C₁-C₁₂ alkyl, C₃-C₁₂alkenyl, C₃-C₁₂ alkynyl, or is C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂alkynyl mono- to polysubstituted by substituents independently selectedfrom the group consisting of halogen, cyano, nitro, hydroxy, mercapto,azido, formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-,(R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—,(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₁₂alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein thegroup B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—,—ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)₂—,—S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—,—C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or

R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, inturn, are mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, mercapto,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

R₅ is selected from A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-,A-(C₃-C₆alkenyl)-, A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-,A-O—(C₄-C₆alkynyl)-, A-(C₃-C₈cycloalkyl)- and A-O—(C₃-C₈cycloalkyl)-;

wherein A is a three- to ten-membered monocyclic or fused bicyclic ringsystem which can be aromatic, partially saturated or fully saturated andcan contain 1 to 4 hetero atoms selected from the group consisting ofnitrogen, oxygen and sulphur, it not being possible for each ring systemto contain —O—O—, —S—S— and —O—S— fragments, and it being possible forthe three- to ten-membered ring system to be itself mono- orpolysubstituted

A1) by substituents independently selected from the group consisting of

halogen, cyano, nitro, hydroxy, mercapto, nitro, azido, formyl, carboxy,═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl,C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, C₃-C₈halocycloalkyloxy, C₃-C₈ cycloalkenyloxy, C₃-C₈ halocycloalkenyloxy,benzyl, benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy,phenyl and phenoxy, in turn, may be mono- to polysubstituted bysubstituents independently selected from the group consisting ofhalogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆ alkylsulfonyl; or

A3) by substituents independently selected from the group consisting of

formyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl,C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇alkynyloxycarbonyl, C₄-C₈ cycloalkoxycarbonyl and benzyloxycarbonyl, andbenzyloxycarbonyl mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, C₁-C₆alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; or

A4) by substituents independently selected from the group consisting ofhydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl,═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionallysubstituted by one or more group selected from the group consisting ofhalogen, methyl, halomethyl; or

R₅ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O, S or Natoms, wherein there are no adjacent O atoms, which is optionallysubstituted by one or more groups independently selected from halogen,CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₂-C₇alkylcarbonyl, C₂-C₇alkoxycarbonyl,C₄-C₇-alkenyloxycarbonyl, C₄-C₇alkynyloxycarbonyl, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R₆ is hydrogen;

R₇ is hydrogen or C₁-C₄ alkyl.

In another group of compounds of formula I, R₁ and R₂ are eachindependently selected from hydrogen or C₁-C₄ alkyl;

or R₁ and R₂ together with the nitrogen atom to which they are attachedform a pyrrolidine or piperidine;

R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, amino,C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino, imidazolino,triazolino, formyl, phenyl, C₂-C₄ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl or C₁-C₆ hydroxyalkyl;

R₄ is selected from fluorine, chlorine, bromine, C₁-C₄ alkyl, C₁-C₄alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, and C₃-C₆ cycloalkyl;

R₅ is selected from G¹, G², G³-G⁴, G⁵, G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹², G¹³,G¹⁴, G¹⁵ and G¹⁶;

R₆ is hydrogen;

R₇ is selected from hydrogen or C₁-C₄ alkyl;

G¹ is a C₈-C₁₀ fused bicyclic ring system which may be saturated orcomprise one carbon-carbon double bond and is optionally substituted byone or more groups independently selected from hydroxyl, C₁-C₄ alkyl,C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl and cyano;

G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or moregroups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH,tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl,sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

G³ is phenyl, which is optionally substituted by one or more groupsindependently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups areoptionally substituted by one or more halogen;

G⁴ is C₃-C₁₂ cycloalkyl which is optionally substituted by one or moregroups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl,C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groupsare optionally substituted by one or more halogen;

G⁵ is C₃-C₇ cycloalkyl, which is optionally substituted by one or moregroups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH,tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl,sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆-alkenyloxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl,C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, phenoxy, —C(═O)NH₂,—C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

G⁶ is phenyl, which must be substituted by at least one fluorine and isoptionally further substituted by one or more groups independentlyselected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃),C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃),SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio,C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

G⁷ is methylene;

G⁸ is

G⁹ is

G¹⁰ is phenyl, which is optionally substituted by one or more groupsindependently selected from hydrogen, halogen, CN, NO₂, OH, SH, CHO,C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy,C₃-C₆ halocycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio,C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆alkylsulfonyl, C₁-C₆ haloalkylsulfonyl, phenyl, 2-phenyl-ethynyl and2-phenyl-ethyl;

G¹¹ is methylene substituted by at least one group independentlyselected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄haloalkoxy;

G¹² is

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, CN, NO₂, OH,SH, CHO, COOH, tri(C₁-C₆ alkyl)silyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl,C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄ C₇ alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl,C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O,—C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂;

G¹⁴ is

G¹⁵ is

G¹⁶ is

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 to 4 members selected from the group consisting ofN, N(R^(69′)), O and S (for example, pyridine, pyrimidine, furan,pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazoleor tetrazole), it not being possible for each ring system to contain—O—O—, —S—S— and —O—S-fragments, and it being possible for the five- tosix-membered ring system to be itself mono- or polysubstituted by groupsselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy,C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl;

R^(1′) is selected from the group consisting of hydrogen, fluorine,C₁-C₄-alkyl, C₁-C₄-haloalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of eachother, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently ofeach other, from the group consisting of hydrogen, halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, phenyl,C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(15′) and R^(16′) are independently selected from the group consistingof hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄alkylthio;

R^(26′) is C(R^(36′))₂, N—OH, N—O—C₁-C₄-alkyl, N—O—C₂-C₄-alkenyl,N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl,N—O-benzyl, N—O-phenyl, N—O-halophenyl, O wherein the N—O-benzyl andN—O-phenyl may be substituted by one or more groups independentlyselected from the group consisting of halogen, methyl and halomethyl;

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′)and R^(35′) are each independently selected from the group consisting ofhydrogen, hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl andphenyl;

or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl;

R^(37′) and R^(38′) are selected independently of each other from thegroup consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(50′) is selected from the group consisting of hydrogen, fluorine,C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected,independently of each other, from the group consisting of hydrogen,fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄alkylthio;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently ofeach other, from the group consisting of hydrogen, halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxy, C₂-C₆ haloalkoxy, phenyl,C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen;

R^(61′) and R^(62′) are selected independently of each other from thegroup consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄haloalkyl;

R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy andC₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(69′) is selected from hydrogen, C₁-C₄ alkyl and C₁-C₄ alkylcarboxy;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r, s and t are independently selected from 0 and 1.

In another group of compounds of formula I, R₁ and R₂ are each C₁-C₄alkyl;

R₃ represents hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl or C₁-C₄ alkylsulfonyl;

R₄ is selected from methyl, ethyl, methoxy, fluorine and chlorine;

R₆ is hydrogen;

R₇ is hydrogen or C₁-C₄ alkyl.

In another group of compounds, R₁ and R₂ are each independently selectedfrom methyl, ethyl and isopropyl;

R₃ represents hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl,cyclopropyl, ethynyl or C₁-C₄ alkoxy;

R₄ is selected from methyl, methoxy, fluorine and chlorine;

R₆ is hydrogen;

R₇ is hydrogen.

In another group of compounds, R₁ is methyl;

R₂ is ethyl;

R₃ is selected from hydrogen, bromine, iodine, methyl, CHF₂,cyclopropyl, ethynyl and methoxy;

R₄ is methyl;

R₆ is hydrogen;

R₇ is hydrogen.

In another group of compounds, G¹ is a C₉-C₁₀ fused bicyclic ring systemwhich may be saturated or comprise one carbon-carbon double bond and isoptionally substituted by one or more groups independently selected fromC₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl;

G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or moregroups independently selected from halogen, ethyl, n-propyl, iso-propyl,n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

G³ is phenyl, which is optionally substituted by one or more groupsindependently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ fluoroalkyl,C₁-C₄ alkoxy and halogen;

G⁴ is C₅-C₆ cycloalkyl which is optionally substituted by one or moregroups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl,C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groupsare optionally substituted by one or more halogen;

G⁵ is C₃-C₇ cycloalkyl, which is substituted by one or more groupsindependently selected from ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy, C₃-C₄-alkenyloxy,phenoxy and C₁-C₆ alkylthio;

G⁶ is phenyl, which must be substituted by at least one fluorine and isoptionally further substituted by one or more groups independentlyselected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃),C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃),SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆ alkylsulfonyl;

G¹⁰ is phenyl, which is optionally substituted by one or more groupsindependently selected from halogen, CN, OH, SH, CHO, methyl, ethyl,n-propyl, iso-propyl, phenyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃,CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃),CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy,iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃, SCH₂CH₃, S(═O)CH₃,S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

G¹¹ is methylene substituted by at least one group independentlyselected from C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄haloalkoxy;

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and ═O;

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 to 4 members selected from the group consisting ofN, N(R^(69′)), O and S (for example, pyridine, pyrimidine, furan,pyrrole, thiazole, oxazole, pyrazole, imidazole, oxadiazole, thiadiazoleor tetrazole), it not being possible for each ring system to contain—O—O—, —S—S— and —O—S-fragments, and it being possible for the five- tosix-membered ring system to be itself mono- or polysubstituted by groupsselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy,C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl;

R^(1′) is selected from the group consisting of hydrogen, fluorine,C₁-C₄ alkyl and C₁-C₄ fluoroalkyl;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of eachother, from the group consisting of hydrogen, fluorine, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently ofeach other, from the group consisting of hydrogen, cyano, halogen, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) andR^(22′) are independently selected from the group consisting ofhydrogen, halogen, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃,CF₂—CH₃ and CF₂CF₃;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄alkylthio;

R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl,N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl,N—O-halophenyl, O, or C(R^(36′))₂;

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′)and R^(35′) are each independently selected from the group consisting ofhydrogen, hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl;

R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) andR^(44′) are selected independently of each other from a group consistingof hydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl,polyfluoromethyl, monofluoroethyl, and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independentlyselected from the group consisting of hydrogen, fluorine, chlorine,bromine, iodine, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,difluoromethoxy, trifluoromethoxy, ethoxy, methlythio, methylsulfinyland methylsulfonyl;

R^(50′) is selected from the group consisting of hydrogen, fluorine,C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected,independently of each other, from the group consisting of hydrogen,fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄haloalkoxy;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently ofeach other, from the group consisting of hydrogen, cyano, halogen, C₁-C₆alkyl and C₁-C₆ haloalkyl;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen;

R^(61′) and R^(62′) are selected independently of each other from thegroup consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄haloalkyl;

R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selectedindependently of each other from the group consisting of hydrogen,fluorine, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄haloalkoxy;

R^(69′) is selected from hydrogen, C₁-C₄ alkyl and C₁-C₄ alkylcarboxy;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r and s are 0 and t is 1 or 0.

In another group of compounds, G¹ is a saturated C₁₀ fused bicyclic ringsystem which is optionally substituted by one or more groupsindependently selected from C₁-C₄ alkyl, fluorine, methoxy and C₁-C₄fluoroalkyl;

G² is a C₅-C₆ cycloalkenyl group optionally substituted by one or morefluorine atoms;

G³ is phenyl, which is optionally substituted by one or more groupsindependently selected from C₁-C₄ alkyl, CHF₂, CF₃, C₁-C₄ alkoxy andhalogen;

G⁴ is C₅-C₆ cycloalkyl which is optionally substituted by one or moregroups independently selected from hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl,C₂-C₄ alkynyl, C₁-C₄ alkoxy and halogen;

G⁵ is C₅-C₆ cycloalkyl, which is substituted by one or more groupsindependently selected from ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂ and C₂-C₆ haloalkyl;

G⁶ is phenyl, which must be substituted by at least one fluorine and isoptionally further substituted by one or more groups independentlyselected from halogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄alkoxy.

G⁷ is methylene;

G¹⁰ is phenyl, which is optionally substituted by one or more groupsindependently selected from hydrogen, halogen, CN, OH, methyl, ethyl,n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃,CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂,C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy, iso-propyloxy,phenyl and OCHF₂;

G¹¹ is methylene substituted by at least one group independentlyselected from C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and ═O;

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 to 4 members selected from the group consisting ofN, N(R^(69′)), O and S it not being possible for each ring system tocontain —O—O—, —S—S— and —O—S— fragments, and it being possible for thefive- to six-membered ring system to be itself mono- or polysubstitutedby groups selected from the group consisting of halogen, CN, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl orbenzyl, wherein the phenyl or benzyl are optionally substituted byhalogen, CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl;

R^(1′) is selected from the group consisting of hydrogen, fluorine,methyl, CH₂F and CF₃;

R^(2′), R^(3′), R^(4′) and R^(5′) are selected, independently of eachother, from the group consisting of hydrogen, fluorine, methyl, CH₂F,CF₃ and methoxy;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, CHF₂, CF₃ and C₁-C₄ alkoxy;

R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) andR^(22′) are each independently selected from hydrogen, fluorine, methyl,ethyl, CH₂F, CHF₂, CF₃ and isopropyl;

R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, methyl, fluorine, chlorine, bromine, ethyl,CH₂F, CHF₂ and CF₃ and isopropyl;

R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl,N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl,N—O-halophenyl, O, C₂-C₄ alkenyloxy or C(R^(36′));

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′)and R^(35′) are each independently selected from the group consisting ofhydrogen, C₁-C₄ alkyl and halogen;

or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl;

R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) andR^(44′) are independently selected from the group consisting ofhydrogen, fluorine, methyl and trifluoromethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independentlyselected from the group consisting of hydrogen, fluorine, chlorine,bromine, iodine, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

R^(50′), R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) areselected, independently of each other, from the group consisting ofhydrogen, fluorine, methyl, CH₂F and CF₃;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, CHF₂ and CF₃;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen;

R^(61′) and R^(62′) are selected independently of each other from thegroup consisting of hydrogen, fluorine, methyl, ethyl, CHF₂ and CF₃;

R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) areselected independently of each of there from the group consisting ofhydrogen, fluoro, methyl, ethyl, methoxy, difluoromethoxy,trifluoromethoxy, CHF₂ and CF₃;

R^(69′) is selected from hydrogen and C₁-C₄ alkyl;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r and s are 0 and t is 1 or 0.

In another group of compounds, G¹ is a saturated C₁₀ fused bicyclic ringsystem;

G² is a C₅-C₆ cycloalkenyl group;

G³ is phenyl;

G⁴ is cyclohexyl or cyclopentyl;

G⁵ is C₆ cycloalkyl, which is substituted by one or more groupsindependently selected from ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂ and—CH(CH₃)—CH(CH₃)₂;

G⁶ is phenyl, which must be substituted by at least one fluorine and isoptionally further substituted by one or more methyl, bromine, iodine orchlorine;

G⁷ is methylene;

G¹⁰ is phenyl, which is optionally substituted by one or more groupsindependently selected from halogen, CN, methyl, ethyl, n-propyl,iso-propyl, ethenyl, methoxy, ethoxy, iso-propyloxy, phenyl, CHF₂, CF₃,CHF—CH₃ and OCHF₂;

G¹¹ is methylene substituted by at least one group independentlyselected from methyl, CF₃ and ethyl;

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, C₁-C₄ alkyl,C₁-C₄ alkoxy and ═O;

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 or 2 members selected from the group consisting ofN, O and S, it not being possible for each ring system to contain —O—O—,—S—S— and —O—S— fragments, and it being possible for the five- tosix-membered ring system to be itself mono- or polysubstituted by groupsselected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl;

R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each hydrogen;

R^(11′), R^(12′), R^(13′) and R^(14′) are selected, independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ alkoxy;

R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′), R^(22′),R^(23′), R^(24′) and R^(25′) are each independently selected fromhydrogen, methyl, ethyl and isopropyl;

R^(23′), R^(24′) and R^(25′) are each independently selected fromhydrogen, fluorine, chlorine, bromine, methyl, ethyl and isopropyl;

R^(26′) is N—OH, N—O—C₁-C₄ alkyl, N—O—C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl,N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl,N—O-halophenyl, O, C₂-C₄ alkenyloxy and C(R^(36′));

R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′)and R^(35′) are each hydrogen or methyl; or R^(27′) and R^(28′) togetherwith the two carbon atoms to which they are attached form a double bond;

each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl;

R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) andR^(44′) are hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are independentlyselected from the group consisting of hydrogen, fluorine, chlorine,methyl, CF₃, CHF₂, CH₂F, methoxy, difluoromethoxy and trifluoromethoxy;

R^(50′), R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) areeach hydrogen;

R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently ofeach other, from the group consisting of hydrogen and halogen;

provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen;

R^(61′), R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) andR^(68′) are hydrogen;

R^(69′) is hydrogen;

n is 0 or 1;

p and q are independently selected from 0 and 1;

r, s and t are each 0.

In another preferred group of compounds, R⁵ is G¹.

In another preferred group of compounds, R⁵ is G².

In another preferred group of compounds, R⁵ is G³-G⁴.

In another preferred group of compounds, R⁵ is G⁵.

In another preferred group of compounds, R⁵ is G⁶-G⁷.

In another preferred group of compounds, R⁵ is G⁸.

In another preferred group of compounds, R⁵ is G⁹.

In another preferred group of compounds, R⁵ is G¹⁰-G¹¹.

In another preferred group of compounds, R⁵ is G¹².

In another preferred group of compounds, R⁵ is G¹³.

In another preferred group of compounds, R⁵ is G¹⁴.

In another preferred group of compounds, R⁵ is G¹⁵.

In another preferred group of compounds, R⁵ is G¹⁶.

In a further group of compounds, R₁ is selected from R^(1a) and R^(1b);

R₂ is methyl;

R₃ is selected from R^(3a), R^(3b), R^(3c), R^(3d), R^(3e), R^(3f),R^(3g), R^(3h), R^(3i), R^(3j), R^(3k), R^(3l), R^(3m), R^(3n), R^(3o),R^(3p), R^(3q), R^(3r), R^(3s), R^(3t);

R₄ is selected from R_(4a), R_(4b), R_(4c), R_(4d), R_(4e), R_(4f);

R₅ is selected from R^(5a), R^(5b), R^(5c), R^(5d), R^(5e), R^(5f),R^(5g), R^(5h), R^(5j), R^(5k), R^(5l), R^(5m), R^(5n), R^(5o), R^(5p),R^(5q), R^(5r), R^(5s), R^(5t), R^(5u), R^(5v), R^(5x), R^(5y), R^(5z),R^(5ab), R^(5ac), R^(5ad), R^(5ae), R^(5af), R^(5ag), R^(5ah), R^(5aj),R^(5ak), R^(5al), R^(5am), R^(5aa), R^(5bb), R^(5cc), R^(5dd), R^(5ee),R^(5ff), R^(5gg), R^(5hh), R^(5jj), R^(5kk), R^(5ll), R^(5mm), R^(5nn),R^(5oo), R^(5pp), R^(5qq), R^(5rr), R^(5ss), R^(5tt), R^(5uu), R^(5vv),R^(5ww), R^(5xx), R^(5zz), R^(5ba), R^(5bc), R^(5bd), R^(5be), R^(5bf),R^(5bg), R^(5bh), R^(5bi), R^(5bj), R^(5bk), R^(5bi), R^(5bm), R^(5bn),R^(5bo), R^(5bp), R^(5bq), R^(5br), R^(5bs), R^(5bt), R^(5bu), R^(5bv),R^(5bw), R^(5bx), R^(5by), R^(5bz), R^(5ca), R^(5cb), R^(5cd), R^(5ce),R^(5cf), R^(5cg), R^(5bh), R^(5ci), R^(5cj), R^(5ck), R^(5cl), R^(5cm),R^(5cn), R^(5co), R^(5cp), R^(5cq), R^(5cr), R^(5cs), R^(5ct), R^(5cu),R^(5cv), R^(5cw), R^(5cx), R^(5cy), R^(5cz), R^(5da), R^(5db), R^(5dc),R^(5de), R^(5df), R^(5dg), R^(5dh), R^(5di), R^(5dj), R^(5dk), R^(5dl),R^(5dm), R^(5dn), R^(5do), R^(5dp), R^(5q), R^(5dr), R^(5ds), R^(5dt),R^(5du), R^(5dv), R^(5dw), R^(5dx), R^(5ea), R^(5eb), R^(5ec), R^(5ed),R^(5ef), R^(5eg), R^(5eh), R^(5ei), R^(5ej), R^(5ek), R^(5ela), R^(5em),R^(5en), R^(5eo), R^(5ep), R^(5eq), R^(5er), R^(5es), R^(5et), R^(5eu),R^(5ev), R^(5ex), R^(5ey), R^(5ez), R^(5fa), R^(5fb), R^(5fc), R^(5fd),R^(5fe), R^(5fg), R^(5fh), R^(5fi), R^(5fj), R^(5fk), R^(5fl), R^(5fm),R^(5fn), R^(5fo), R^(5fp), R^(5fq), R^(5fr), R^(5fs), R^(5ft), R^(5fu),R^(5fv), R^(5fw);

R₆ is selected from R^(a), R^(b) and R^(c);

R₇ is H;

R^(1a) is selected from ethyl and isopropyl;

R^(1b) is ethyl;

R^(3a) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,CCH, CH═CH₂, H₂C═C—(CH₃), cyclopropyl, halomethyl, haloethyl, methoxy,halomethoxy, ethoxy, haloethoxy, methlythio, halomethylthio,methylsulfinyl, halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl,amino, methylamino, dimethylamino, ethylamino, diethylamino,ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO, CH₂OH,CH(OH)Me and CO-Me;

R^(3b) is selected from hydrogen, F, Cl, Br, I, cyano, methyl, ethyl,isopropyl, fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF,methoxy and ethoxy;

R^(3c) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl,fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF, methoxy andethoxy;

R^(3d) is selected from hydrogen, halogen, cyano, methyl, ethyl,isopropyl, C≡CH, CH═CH₂, H₂C═C—(CH₃), cyclopropyl, halomethyl,haloethyl, methoxy, ethoxy, methlythio, halomethylthio, methylsulfinyl,halomethylsulfinyl, methylsulfonyl, halomethylsulfonyl,

amino, methylamino, dimethylamino, ethylamino, diethylamino,ethylmethylamino, pyrrolidino, imidazolino, triazolino, CHO and CO-Me;

R^(3b) is selected from hydrogen, F, Cl, Br, I, cyano, methyl, ethyl,isopropyl, fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF,methoxy and ethoxy;

R^(3c) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl,fluoromethyl, difluoromethyl, trifluoromethyl, (H₃C)—CHF, methoxy andethoxy;

R^(3e) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy,ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl,methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino,ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino,triazolino, CHO, CH₂OH, CH(OH)Me and CO-Me;

R^(3f) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy,ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

R^(3g) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃,—CF₂—CH₃, methoxy, ethoxy, methlythio, methylsulfinyl andmethylsulfonyl;

R^(3h) is selected from hydrogen, Br, I, methyl, ethyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F and methoxy;

R^(3i) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy,ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl,methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino,ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino,triazolino, CHO and CO-Me;

R^(3j) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,halomethyl, haloethyl, methoxy and ethoxy;

R^(3k) is selected from hydrogen, halogen, methyl, ethyl, isopropyl,CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, methoxy and ethoxy;

R^(3l) is selected from hydrogen, halogen, methyl, ethyl, isopropyl,CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, methoxy and ethoxy;

R^(3m) is selected from hydrogen, F, Br, I, methyl, ethyl, CHF₂ andmethoxy;

R^(3n) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy,ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl,methylsulfonyl, halomethylsulfonyl, amino, methylamino, dimethylamino,ethylamino, diethylamino, ethylmethylamino, pyrrolidino, imidazolino,triazolino, CHO, CH₂OH, CH(OH)Me and CO-Me;

R^(3o) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxy,ethoxy, methlythio, halomethylthio, methylsulfinyl, halomethylsulfinyl,methylsulfonyl and halomethylsulfonyl;

R^(3p) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl, haloethyl, methoxyand ethoxy;

R^(3q) is selected from hydrogen, F, Br, I, methyl, ethyl, isopropyl,cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃,—CF₂—CH₃, methoxy, ethoxy, methlythio, methylsulfinyl andmethylsulfonyl;

R^(3r) is selected from hydrogen, Br, I, methyl, cyclopropyl, C≡CH,CH═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃ and methoxy;

R^(3s) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,cyclopropyl, tert-butyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl,haloethyl, methoxy, halomethoxy, ethoxy, haloethoxy, methlythio,halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl,halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino,diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino,CHO and C(═O)Me;

R^(3t) is selected from hydrogen, halogen, CN, methyl, ethyl, isopropyl,cyclopropyl, tert-butyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, halomethyl,haloethyl, methoxy, halomethoxy, ethoxy, haloethoxy, methlythio,halomethylthio, methylsulfinyl, halomethylsulfinyl, methylsulfonyl,halomethylsulfonyl, amino, methylamino, dimethylamino, ethylamino,diethylamino, ethylmethylamino, pyrrolidino, imidazolino, triazolino,CHO and C(═O)Me;

R_(4a) is selected from F, Cl, Br, C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄haloalkyl and C₁-C₄ cycloalkyl;

R_(4b) is selected from F, Cl, methyl, ethyl, ethenyl, propyl, propenyl,isopropyl, isopropenyl, cyclopropanyl, methoxy, ethoxy,monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoromethyl

R_(4c) is selected from methyl, ethyl, methoxy, F and Cl;

R_(4d) is selected from methyl, methoxy, F and Cl;

R_(4e) is selected from methyl;

R_(4f) is selected from methoxy, F and Cl;

R^(5a) is a 3- to 6-membered cycloalkenyl group, or a 3- to 6-memberedcycloalkenyl group that can be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, CN, NO₂,OH, SH, CHO, COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl,n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆alkoxy,C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5b) is a 3- to 6-membered cycloalkenyl group, or a 3- to 6-memberedcycloalkenyl group that can be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, ethyl,n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl,n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃,—CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5c) is a 3- to 6-membered cycloalkenyl group, or a 3- to 6-memberedcycloalkenyl group that can be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, ethyl,n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl,n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃,—CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂,C₁-C₆-fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5d) is a 5-membered cycloalkenyl group, or a 5-membered cycloalkenylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5e) is a 5-membered cycloalkenyl group, or a 5-membered cycloalkenylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

R^(5f) is a 5-membered cycloalkenyl group, or a 5-membered cycloalkenylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆-fluoroalkyl, C₁-C₆ alkoxyand C₁-C₆ alkylthio;

R^(59g) is a 6-membered cycloalkenyl group, or a 6-membered cycloalkenylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄ C₇alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5h) is a 6-membered cycloalkenyl group, or a 6-membered cycloalkenylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

R^(5j) is a 6-membered cycloalkenyl group, or a 6-membered cycloalkenylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxyand C₁-C₆ alkylthio;

R^(5k) is a 3- to 7-membered cycloalkyl group, or a 3- to 7-memberedcycloalkyl group that can be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, CN, NO₂,OH, SH, CHO, COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl,n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5l) is a 3- to 7-membered cycloalkyl group, or a 3- to 7-memberedcycloalkyl group that can be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, ethyl,n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl,n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃,—CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆haloalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5m) is a 3- to 7-membered cycloalkyl group, or a 3- to 7-memberedcycloalkyl group that can be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, ethyl,n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl,n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃,—CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂,C₁-C₆-fluoroalkyl, C₁-C₆ alkoxy and C₁-C₆ alkylthio;

R^(5n) is a 3-membered cycloalkyl group, or a 3-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄ C₇alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5o) is a 3-membered cycloalkyl group, or a 3-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

R^(5p) is a 3-membered cycloalkyl group, or a 3-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxyand C₁-C₆ alkylthio;

R^(5q) is a 4-membered cycloalkyl group, or a 4-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄ C₇alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5r) is a 4-membered cycloalkyl group, or a 4-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

R^(5s) is a 4-membered cycloalkyl group, or a 4-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxyand C₁-C₆ alkylthio;

R^(5t) is a 5-membered cycloalkyl group, or a 5-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄ C₇alkenyloxycarbonyl, C₄ C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5u) is a 5-membered cycloalkyl group, or a 5-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

R^(5v) is a 5-membered cycloalkyl group, or a 5-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxyand C₁-C₆ alkylthio;

R^(5x) is a 6-membered cycloalkyl group, or a 6-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,COOH, tri(C₁-C₆alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5y) is a 6-membered cycloalkyl group, or a 6-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

R^(5z) is a 6-membered cycloalkyl group, or a 6-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxyand C₁-C₆ alkylthio;

R^(5ab) is a 7-membered cycloalkyl group, or a 7-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, CN, NO₂, OH, SH, CHO,COOH, tri(C₁-C₆ alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂;

R^(5ac) is a 7-membered cycloalkyl group, or a 7-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio;

R^(5ad) is a 7-membered cycloalkyl group, or a 7-membered cycloalkylgroup that can be mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₁-C₆ fluoroalkyl, C₁-C₆ alkoxyand C₁-C₆ alkylthio;

R^(5ae) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachindependently selected from hydrogen, fluoro, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl;

R^(5af) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachindependently selected from hydrogen, fluoro, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy and C₁-C₄ alkylthio;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy and C₁-C₆ alkylthio;

R^(5ag) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachindependently selected from hydrogen, fluoro, methyl, ethyl, CH₂F, CHF₂,CF₃, CHF—CH₃, CF₂—CH₃, methoxy, ethoxy, S—CH₃ and S—CH₂CH₃;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy and C₁-C₄ alkylthio;

R^(5ah) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachindependently selected from hydrogen, fluoro, methyl, CHF₂, CF₃ andmethoxy;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl;

R^(5aj) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachindependently selected from hydrogen, fluoro, methyl, CHF₂, CF₃ andmethoxy;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy and C₁-C₆ alkylthio;

R^(5ak) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachindependently selected from hydrogen, fluoro, methyl, CHF₂, CF₃ andmethoxy;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy and C₁-C₄ alkylthio;

R^(5al) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachhydrogen;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl;

R^(5am) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachhydrogen;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy and C₁-C₆ alkylthio;

R^(5aa) is G⁸ wherein R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are eachhydrogen;

and wherein R^(11′), R^(12′), R^(13′) and R^(14′) are each independentlyselected from hydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy and C₁-C₄ alkylthio;

R^(5bb) is a benzyl group, wherein the phenyl ring is substituted by atleast one fluorine and optionally by one or more groups independentlyselected from the group consisting of hydrogen, halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy,C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl;

R^(5cc) is a benzyl group, wherein the phenyl ring is substituted by atleast one fluorine and optionally by one or more groups independentlyselected from the group consisting of hydrogen, halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆alkynyloxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl;

R^(5dd) is a benzyl group, wherein the phenyl ring is substituted by atleast one fluorine and optionally by one or more groups independentlyselected from the group consisting of hydrogen, halogen, CN, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl,C₁-C₆ alkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy and C₁-C₆ alkylthio;

R^(5ee) is a benzyl group, wherein the phenyl ring is substituted by atleast one fluorine and optionally by one or more groups independentlyselected from the group consisting of hydrogen, halogen, CN, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₃-C₆ cycloalkyl and C₁-C₄alkoxy;

R^(5ff) is a benzyl group, wherein the methylene portion is substitutedby at least one group independently selected from the group consistingof hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄haloalkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5gg) is a benzyl group, wherein the methylene portion is substitutedby at least one group independently selected from the group consistingof hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy,C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5hh) is a benzyl group, wherein the methylene portion is substitutedone group independently selected from the group consisting of C₁-C₄alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl

R^(5jj) is a benzyl group, wherein the methylene portion is substitutedby one group independently selected from the group consisting ofhydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy,C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5kk) is a benzyl group, wherein the methylene portion is substitutedone group independently selected from the group consisting of methyl,ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5ll) is a benzyl group, wherein the methylene portion is substitutedby one group independently selected from the group consisting of methyl,ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy,C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

R^(5mm) is a benzyl group, wherein the methylene portion is substitutedby at least one group independently selected from the group consistingof hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄haloalkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, OH, SH, CHO C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl;

R^(5nn) is a benzyl group, wherein the methylene portion is substitutedone group independently selected from the group consisting of C₁-C₄alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, OH, SH, CHO C_(r) C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆cycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl;

R^(oo) is a benzyl group, wherein the methylene portion is substitutedone group independently selected from the group consisting of methyl,ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, OH, SH, CHO C_(r) C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆cycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl;

R^(5pp) is a benzyl group, wherein the methylene portion is substitutedby at least one group independently selected from the group consistingof hydrogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄haloalkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, CH₂F,CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂,CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂,C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH,SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

R^(5qq) is a benzyl group, wherein the methylene portion is substitutedone group independently selected from the group consisting of C₁-C₄alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, CH₂F,CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂,CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂,C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH,SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

R^(5rr) is a benzyl group, wherein the methylene portion is substitutedone group independently selected from the group consisting of methyl,ethyl, CHF₂, CF₃ and methoxy;

and wherein the phenyl ring is optionally substituted by one or moregroups independently selected from the group consisting of hydrogen,halogen, CN, OH, SH, CHO, methyl, ethyl, n-propyl, iso-propyl, CH₂F,CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂,CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂,C≡CH, methoxy, ethoxy, iso-propyloxy, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH,SCH₃, SCH₂CH₃, S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃;

R^(5ss) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

R^(5tt) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5vv) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5vv) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5ww) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5xx) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′)are hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is either 0 or 1;

R^(5zz) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, fluoromethyl and fluoroethyl;

R^(5ba) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is either 0 or 1;

R^(5bc) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is either 0 or 1;

R^(5bd) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(22′) to R^(24′) are selected independently of each other, from thegroup consisting of hydrogen, cyano, halogen, methyl, ethyl, isopropyl,monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is either 0 or 1;

R^(5be) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is either 0 or 1;

R^(5bf) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) ishydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is either 0 or 1;

R^(5bg) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(5bh) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is either 0 or 1;

R^(5bi) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is either 0 or 1;

R^(5bj) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is either 0 or 1;

R^(5bk) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is either 0 or 1;

R^(5bl) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) ishydrogen;

R^(22′) to R^(24′) are selected independently of each other, from thegroup consisting of hydrogen, F, Cl, Br, methyl, ethyl, isopropyl, CH₂F,CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

n is either 0 or 1;

R^(5bm) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 0;

R^(5bn) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 0;

R^(5bo) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 0;

R^(5bp) P is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 0;

R^(5bq) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 0;

R^(5br) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) isselected independently of each other, from the group consisting ofhydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 0;

R^(5bs) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 0;

R^(5bt) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 0;

R^(5bu) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 0;

R^(5bv) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 0;

R^(5bw) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 0;

R^(5bx) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) ishydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 0;

R^(5by) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 0;

R^(5bz) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 0;

R^(5ca) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 0;

R^(5cb) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 0;

R^(5cd) is G⁹ wherein R^(23′), R^(24′) and R^(25′) are selectedindependently of each other, from the group consisting of methyl, F andCF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 0;

R^(5ce) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) ishydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 0;

R^(5cf) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 1;

R^(5cg) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 1;

R^(5ch) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 1;

R^(5ci) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 1;

R^(5cj) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 1;

R^(5ck) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) isselected independently of each other, from the group consisting ofhydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyland C₁-C₄ alkylthio;

n is 1;

R^(5cl) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 1;

R^(5cm) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 1;

R^(5cn) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 1;

R^(5co) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 1;

R^(5cp) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 1;

R^(5cq) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) ishydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, cyano, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

n is 1;

R^(5cr) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 1;

R^(5cs) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl, andpolyfluoroethyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 1;

R^(5ct) is G⁹ wherein each R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 1;

R^(5cu) is G⁹ wherein R^(15′), R^(16′), R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are each hydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 1;

R^(5cv) is G⁹ wherein R^(15′) and R^(16′) are selected independently ofeach other, from the group consisting of methyl, F and CF₃;

each R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areselected independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 1;

R^(5cw) is G⁹ wherein R^(15′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₃-C₆cycloalkyl;

each R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) ishydrogen;

R^(23′), R^(24′) and R^(25′) are selected independently of each other,from the group consisting of hydrogen, F, Cl, Br, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

n is 1;

R^(5cx) is G¹⁴ wherein G¹⁴ is

wherein R^(37′) and R^(38′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl andC₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy andC₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5cy) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5cz) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5da) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5db) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dc) is G¹⁴ wherein R^(37′) is selected independently of each otherfrom the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl andC₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5de) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′), and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy andC₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5df) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoromethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dg) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dh) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and 44′ are selected independently of each other fromthe group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5di) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dj) is G¹⁴ wherein R^(37′) is selected independently of each otherfrom the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl andC₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are independently selected from 0 and 1;

R^(5dk) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy andC₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dl) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(42′),R^(43′) and R^(44′) are selected independently of each other from thegroup consisting of hydrogen, halogen, methyl, ethyl, isopropyl,monofluoromethyl, polyfluoromethyl, monofluoroethyl and polyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dm) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dn) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5do) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dp) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are independently selected from 0 and 1;

R^(5dq) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, andC₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dr) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5ds) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dt) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5du) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dv) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p and q are each 0;

R^(5dw) is G¹⁴ wherein R^(37′) and R^(37′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5dx) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ea) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(eb) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently from each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ec) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ed) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p and q are each 0;

R^(5ef) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5eg) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5eh) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5ei) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5ej) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p and q are each 0;

R^(5ek) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5el) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5em) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5en) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5eo) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are independently selected of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5ep) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5eq) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 0;

q is 1;

R^(5er) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5es) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5et) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5eu) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′), and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5ev) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selectedindependently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5ex) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) selected, independentlyof each other, from the group consisting of hydrogen, F, Cl, Br, I,methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃,CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, trifluoromethoxy, ethoxy,methlythio, methylsulfinyl and methylsulfonyl;

p is 0;

q is 1;

R^(5ey) is G¹⁴ wherein R³⁷ and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5ez) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoromethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fa) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fb) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fc) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fd) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 0;

q is 1;

R^(5fe) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fg) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fh) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fi) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fj) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fk) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areeach hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;

p is 1;

q is 1;

R^(5fl) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fm) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fn) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fo) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fp) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(41′), R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fq) is G¹⁴ wherein R^(37′) is selected from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) arehydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, Br, I, methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂,C(CH₃)═CH₂, CF₃, CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy,trifluoromethoxy, ethoxy, methlythio, methylsulfinyl and methylsulfonyl;

p is 1;

q is 1;

R^(5fr) is G¹⁴ wherein R^(37′) and R^(38′) are selected independently ofeach other from the group consisting of hydrogen, halogen, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl;

R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₁-C₄ haloalkoxy and C₁-C₄ alkylthio;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fs) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, halogen, methyl, ethyl,isopropyl, monofluoromethyl, polyfluoromethyl, monofluoroethyl andpolyfluoroethyl;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5ft) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are selected independently of each otherfrom the group consisting of hydrogen, fluorine, methyl, ethyl,isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ andCH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fu) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44″) are selected independently of each otherfrom the group consisting of methyl, ethyl, F and CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fv) is G¹⁴ wherein R^(37′), R^(38′), R^(39′), R^(40′), R^(41′),R^(42′), R^(43′) and R^(44′) are each hydrogen;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(5fw) is G¹⁴ wherein R^(37′) is selected from hydrogen, halogen,cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl;

R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areselected independently of each other from the group consisting ofhydrogen, fluorine, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃, CHF—CH₃,CF₂—CH₃, CH₂—CH₂F CH₂—CHF₂ and CH₂—CF₃;

R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen, F,Cl, methyl, CF₃, CHF₂, CH₂F, methoxy and trifluoromethoxy;

p is 1;

q is 1;

R^(6a) is selected from hydrogen and SH;

R^(6b) is hydrogen;

R^(6c) is SH.

Each line of Table N describes a preferred sub-group from N1-N757 ofthis group. For reasons of clarity, note that in these sub-groups, R₂ isalways methyl and R₇ is always hydrogen. For example, sub-group N1 is agroup of compounds of formula (I) wherein

R₁ is R^(1b);

R₂ is methyl;

R₃ is R^(3a);

R₄ is R^(4c);

R₅ is R^(5a);

R₆ is R^(6b);

R₇ is H.

TABLE N R₁ R₃ R₄ R₅ R₆ N1 R^(1b) R^(3a) R^(4c) R^(5a) R^(6b) N2 R^(1b)R^(3b) R^(4d) R^(5a) R^(6b) N3 R^(1b) R^(3c) R^(4e) R^(5a) R^(6b) N4R^(1b) R^(3a) R^(4c) R^(5b) R^(6b) N5 R^(1b) R^(3b) R^(4d) R^(5b) R^(6b)N6 R^(1b) R^(3c) R^(4e) R^(5b) R^(6b) N7 R^(1b) R^(3a) R^(4c) R^(5c)R^(6b) N8 R^(1b) R^(3b) R^(4d) R^(5c) R^(6b) N9 R^(1b) R^(3c) R^(4e)R^(5c) R^(6b) N10 R^(1b) R^(3a) R^(4c) R^(5d) R^(6b) N11 R^(1b) R^(3b)R^(4d) R^(5d) R^(6b) N12 R^(1b) R^(3c) R^(4e) R^(5d) R^(6b) N13 R^(1b)R^(3a) R^(4c) R^(5e) R^(6b) N14 R^(1b) R^(3b) R^(4d) R^(5e) R^(6b) N15R^(1b) R^(3c) R^(4e) R^(5e) R^(6b) N16 R^(1b) R^(3a) R^(4c) R^(5f)R^(6b) N17 R^(1b) R^(3b) R^(4d) R^(5f) R^(6b) N18 R^(1b) R^(3c) R^(4e)R^(5f) R^(6b) N19 R^(1b) R^(3a) R^(4c) R^(5g) R^(6b) N20 R^(1b) R^(3b)R^(4d) R^(5g) R^(6b) N21 R^(1b) R^(3c) R^(4e) R^(5g) R^(6b) N22 R^(1b)R^(3a) R^(4c) R^(5h) R^(6b) N23 R^(1b) R^(3b) R^(4d) R^(5h) R^(6b) N24R^(1b) R^(3c) R^(4e) R^(5h) R^(6b) N25 R^(1b) R^(3a) R^(4c) R^(5j)R^(6b) N26 R^(1b) R^(3b) R^(4d) R^(5j) R^(6b) N27 R^(1b) R^(3c) R^(4e)R^(5j) R^(6b) N28 R^(1b) R^(3d) R^(4c) R^(5k) R^(6b) N29 R^(1b) R^(3b)R^(4d) R^(5k) R^(6b) N30 R^(1b) R^(3c) R^(4e) R^(5k) R^(6b) N31 R^(1b)R^(3d) R^(4c) R^(5l) R^(6b) N32 R^(1b) R^(3b) R^(4d) R^(5l) R^(6b) N33R^(1b) R^(3c) R^(4e) R^(5l) R^(6b) N34 R^(1b) R^(3d) R^(4c) R^(5m)R^(6b) N35 R^(1b) R^(3b) R^(4d) R^(5m) R^(6b) N36 R^(1b) R^(3c) R^(4e)R^(5m) R^(6b) N37 R^(1b) R^(3d) R^(4c) R^(5n) R^(6b) N38 R^(1b) R^(3b)R^(4d) R^(5n) R^(6b) N39 R^(1b) R^(3c) R^(4e) R^(5n) R^(6b) N40 R^(1b)R^(3d) R^(4c) R^(5o) R^(6b) N41 R^(1b) R^(3b) R^(4d) R^(5o) R^(6b) N42R^(1b) R^(3c) R^(4e) R^(5o) R^(6b) N43 R^(1b) R^(3d) R^(4c) R^(5p)R^(6b) N44 R^(1b) R^(3b) R^(4d) R^(5p) R^(6b) N45 R^(1b) R^(3c) R^(4e)R^(5p) R^(6b) N46 R^(1b) R^(3d) R^(4c) R^(5q) R^(6b) N47 R^(1b) R^(3b)R^(4d) R^(5q) R^(6b) N48 R^(1b) R^(3c) R^(4e) R^(5q) R^(6b) N49 R^(1b)R^(3d) R^(4c) R^(5r) R^(6b) N50 R^(1b) R^(3b) R^(4d) R^(5r) R^(6b) N51R^(1b) R^(3c) R^(4e) R^(5r) R^(6b) N52 R^(1b) R^(3d) R^(4c) R^(5s)R^(6b) N53 R^(1b) R^(3b) R^(4d) R^(5s) R^(6b) N54 R^(1b) R^(3c) R^(4e)R^(5s) R^(6b) N55 R^(1b) R^(3d) R^(4c) R^(5t) R^(6b) N56 R^(1b) R^(3b)R^(4d) R^(5t) R^(6b) N57 R^(1b) R^(3c) R^(4e) R^(5t) R^(6b) N58 R^(1b)R^(3d) R^(4c) R^(5u) R^(6b) N59 R^(1b) R^(3b) R^(4d) R^(5u) R^(6b) N60R^(1b) R^(3c) R^(4e) R^(5u) R^(6b) N61 R^(1b) R^(3d) R^(4c) R^(5v)R^(6b) N62 R^(1b) R^(3b) R^(4d) R^(5v) R^(6b) N63 R^(1b) R^(3c) R^(4e)R^(5v) R^(6b) N64 R^(1b) R^(3d) R^(4c) R^(5x) R^(6b) N65 R^(1b) R^(3b)R^(4d) R^(5x) R^(6b) N66 R^(1b) R^(3c) R^(4e) R^(5x) R^(6b) N67 R^(1b)R^(3d) R^(4c) R^(5y) R^(6b) N68 R^(1b) R^(3b) R^(4d) R^(5y) R^(6b) N69R^(1b) R^(3c) R^(4e) R^(5y) R^(6b) N70 R^(1b) R^(3d) R^(4c) R^(5z)R^(6b) N71 R^(1b) R^(3b) R^(4d) R^(5z) R^(6b) N72 R^(1b) R^(3c) R^(4e)R^(5z) R^(6b) N73 R^(1b) R^(3d) R^(4c) R^(5ab) R^(6b) N74 R^(1b) R^(3b)R^(4d) R^(5ab) R^(6b) N75 R^(1b) R^(3c) R^(4e) R^(5ab) R^(6b) N76 R^(1b)R^(3d) R^(4c) R^(5ac) R^(6b) N77 R^(1b) R^(3b) R^(4d) R^(5ac) R^(6b) N78R^(1b) R^(3c) R^(4e) R^(5ac) R^(6b) N79 R^(1b) R^(3d) R^(4c) R^(5ad)R^(6b) N80 R^(1b) R^(3b) R^(4d) R^(5ad) R^(6b) N81 R^(1b) R^(3c) R^(4e)R^(5ad) R^(6b) N82 R^(1b) R^(3e) R^(4c) R^(5bb) R^(6b) N83 R^(1b) R^(3f)R^(4c) R^(5bb) R^(6b) N84 R^(1b) R^(3g) R^(4e) R^(5bb) R^(6b) N85 R^(1b)R^(3h) R^(4e) R^(5bb) R^(6b) N86 R^(1b) R^(3e) R^(4c) R^(5cc) R^(6b) N87R^(1b) R^(3f) R^(4c) R^(5cc) R^(6b) N88 R^(1b) R^(3g) R^(4e) R^(5cc)R^(6b) N89 R^(1b) R^(3h) R^(4e) R^(5cc) R^(6b) N90 R^(1b) R^(3e) R^(4c)R^(5dd) R^(6b) N91 R^(1b) R^(3f) R^(4c) R^(5dd) R^(6b) N92 R^(1b) R^(3g)R^(4e) R^(5dd) R^(6b) N93 R^(1b) R^(3h) R^(4e) R^(5dd) R^(6b) N94 R^(1b)R^(3e) R^(4c) R^(5ee) R^(6b) N95 R^(1b) R^(3f) R^(4c) R^(5ee) R^(6b) N96R^(1b) R^(3g) R^(4e) R^(5ee) R^(6b) N97 R^(1b) R^(3h) R^(4e) R^(5ee)R^(6b) N98 R^(1b) R^(3i) R^(4c) R^(5ae) R^(6a) N99 R^(1b) R^(3j) R^(4c)R^(5af) R^(6b) N100 R^(1b) R^(3k) R^(4c) R^(5ag) R^(6a) N101 R^(1b)R^(3k) R^(4c) R^(5ag) R^(6b) N102 R^(1b) R^(3l) R^(4c) R^(5ag) R^(6c)N103 R^(1b) R^(3i) R^(4e) R^(5ae) R^(6a) N104 R^(1b) R^(3j) R^(4e)R^(5af) R^(6b) N105 R^(1b) R^(3k) R^(4e) R^(5ag) R^(6a) N106 R^(1b)R^(3k) R^(4e) R^(5ag) R^(6b) N107 R^(1b) R^(3l) R^(4e) R^(5ag) R^(6c)N108 R^(1b) R^(3i) R^(4f) R^(5ae) R^(6a) N109 R^(1b) R^(3j) R^(4f)R^(5af) R^(6b) N110 R^(1b) R^(3k) R^(4f) R^(5ag) R^(6a) N111 R^(1b)R^(3k) R^(4f) R^(5ag) R^(6b) N112 R^(1b) R^(3l) R^(4f) R^(5ag) R^(6c)N113 R^(1b) R^(3m) R^(4c) R^(5ae) R^(6a) N114 R^(1b) R^(3m) R^(4c)R^(5af) R^(6b) N115 R^(1b) R^(3m) R^(4c) R^(5ag) R^(6a) N116 R^(1b)R^(3m) R^(4c) R^(5ag) R^(6b) N117 R^(1b) R^(3m) R^(4c) R^(5ag) R^(6c)N118 R^(1b) R^(3m) R^(4e) R^(5ae) R^(6a) N119 R^(1b) R^(3m) R^(4e)R^(5af) R^(6b) N120 R^(1b) R^(3m) R^(4e) R^(5ag) R^(6a) N121 R^(1b)R^(3m) R^(4e) R^(5ag) R^(6b) N122 R^(1b) R^(3m) R^(4e) R^(5ag) R^(6c)N123 R^(1b) R^(3m) R^(4f) R^(5ae) R^(6a) N124 R^(1b) R^(3m) R^(4f)R^(5af) R^(6b) N125 R^(1b) R^(3m) R^(4f) R^(5ag) R^(6a) N126 R^(1b)R^(3m) R^(4f) R^(5ag) R^(6b) N127 R^(1b) R^(3m) R^(4f) R^(5ag) R^(6c)N128 R^(1b) R^(3i) R^(4c) R^(5ah) R^(6a) N129 R^(1b) R^(3j) R^(4c)R^(5ai) R^(6b) N130 R^(1b) R^(3k) R^(4c) R^(5ak) R^(6a) N131 R^(1b)R^(3k) R^(4c) R^(5ak) R^(6b) N132 R^(1b) R^(3l) R^(4c) R^(5ak) R^(6c)N133 R^(1b) R^(3i) R^(4e) R^(5ah) R^(6a) N134 R^(1b) R^(3j) R^(4e)R^(5ai) R^(6b) N135 R^(1b) R^(3k) R^(4e) R^(5ak) R^(6a) N136 R^(1b)R^(3k) R^(4e) R^(5ak) R^(6b) N137 R^(1b) R^(3l) R^(4e) R^(5ak) R^(6c)N138 R^(1b) R^(3i) R^(4f) R^(5ah) R^(6a) N139 R^(1b) R^(3j) R^(4f)R^(5ai) R^(6b) N140 R^(1b) R^(3k) R^(4f) R^(5ak) R^(6a) N141 R^(1b)R^(3k) R^(4f) R^(5ak) R^(6b) N142 R^(1b) R^(3l) R^(4f) R^(5ak) R^(6c)N143 R^(1b) R^(3m) R^(4c) R^(5ah) R^(6a) N144 R^(1b) R^(3m) R^(4c)R^(5ai) R^(6b) N145 R^(1b) R^(3m) R^(4c) R^(5ak) R^(6a) N146 R^(1b)R^(3m) R^(4c) R^(5ak) R^(6b) N147 R^(1b) R^(3m) R^(4c) R^(5ak) R^(6c)N148 R^(1b) R^(3m) R^(4e) R^(5ah) R^(6a) N149 R^(1b) R^(3m) R^(4e)R^(5ai) R^(6b) N150 R^(1b) R^(3m) R^(4e) R^(5ak) R^(6a) N151 R^(1b)R^(3m) R^(4e) R^(5ak) R^(6b) N152 R^(1b) R^(3m) R^(4e) R^(5ak) R^(6c)N153 R^(1b) R^(3m) R^(4f) R^(5ah) R^(6a) N154 R^(1b) R^(3m) R^(4f)R^(5ai) R^(6b) N155 R^(1b) R^(3m) R^(4f) R^(5ak) R^(6a) N156 R^(1b)R^(3m) R^(4f) R^(5ak) R^(6b) N157 R^(1b) R^(3m) R^(4f) R^(5ak) R^(6c)N158 R^(1b) R^(3i) R^(4c) R^(5al) R^(6a) N159 R^(1b) R^(3j) R^(4c)R^(5am) R^(6b) N160 R^(1b) R^(3k) R^(4c) R^(5an) R^(6a) N161 R^(1b)R^(3k) R^(4c) R^(5an) R^(6b) N162 R^(1b) R^(3l) R^(4c) R^(5an) R^(6c)N163 R^(1b) R^(3i) R^(4e) R^(5al) R^(6a) N164 R^(1b) R^(3j) R^(4e)R^(5am) R^(6b) N165 R^(1b) R^(3k) R^(4e) R^(5an) R^(6a) N166 R^(1b)R^(3k) R^(4e) R^(5an) R^(6b) N167 R^(1b) R^(3l) R^(4e) R^(5an) R^(6c)N168 R^(1b) R^(3i) R^(4f) R^(5al) R^(6a) N169 R^(1b) R^(3j) R^(4f)R^(5am) R^(6b) N170 R^(1b) R^(3k) R^(4f) R^(5an) R^(6a) N171 R^(1b)R^(3k) R^(4f) R^(5an) R^(6b) N172 R^(1b) R^(3l) R^(4f) R^(5an) R^(6c)N173 R^(1b) R^(3n) R^(4c) R^(5ff) R^(6a) N174 R^(1b) R^(3o) R^(4c)R^(5gg) R^(6b) N175 R^(1b) R^(3o) R^(4c) R^(5gg) R^(6c) N176 R^(1b)R^(3p) R^(4e) R^(5ff) R^(6b) N177 R^(1b) R^(3p) R^(4e) R^(5gg) R^(6b)N178 R^(1b) R^(3q) R^(4e) R^(5ff) R^(6b) N179 R^(1b) R^(3q) R^(4e)R^(5gg) R^(6b) N180 R^(1b) R^(3r) R^(4e) R^(5ff) R^(6b) N181 R^(1b)R^(3r) R^(4e) R^(5gg) R^(6b) N182 R^(1b) R^(3n) R^(4c) R^(5hh) R^(6a)N183 R^(1b) R^(3o) R^(4c) R^(5jj) R^(6b) N184 R^(1b) R^(3o) R^(4c)R^(5jj) R^(6c) N185 R^(1b) R^(3p) R^(4e) R^(5hh) R^(6b) N186 R^(1b)R^(3p) R^(4e) R^(5jj) R^(6b) N187 R^(1b) R^(3q) R^(4e) R^(5hh) R^(6b)N188 R^(1b) R^(3q) R^(4e) R^(5jj) R^(6b) N189 R^(1b) R^(3r) R^(4e)R^(5hh) R^(6b) N190 R^(1b) R^(3r) R^(4e) R^(5jj) R^(6b) N191 R^(1b)R^(3n) R^(4c) R^(5kk) R^(6a) N192 R^(1b) R^(3o) R^(4c) R^(5ll) R^(6b)N193 R^(1b) R^(3o) R^(4c) R^(5ll) R^(6c) N194 R^(1b) R^(3p) R^(4e)R^(5kk) R^(6b) N195 R^(1b) R^(3p) R^(4e) R^(5ll) R^(6b) N196 R^(1b)R^(3q) R^(4e) R^(5kk) R^(6b) N197 R^(1b) R^(3q) R^(4e) R^(5ll) R^(6b)N198 R^(1b) R^(3r) R^(4e) R^(5kk) R^(6b) N199 R^(1b) R^(3r) R^(4e)R^(5ll) R^(6b) N200 R^(1b) R^(3n) R^(4c) R^(5mm) R^(6a) N201 R^(1b)R^(3o) R^(4c) R^(5nn) R^(6b) N202 R^(1b) R^(3o) R^(4c) R^(5nn) R^(6c)N203 R^(1b) R^(3p) R^(4e) R^(5mm) R^(6b) N204 R^(1b) R^(3p) R^(4e)R^(5nn) R^(6b) N205 R^(1b) R^(3q) R^(4e) R^(5mm) R^(6b) N206 R^(1b)R^(3q) R^(4e) R^(5nn) R^(6b) N207 R^(1b) R^(3r) R^(4e) R^(5mm) R^(6b)N208 R^(1b) R^(3r) R^(4e) R^(5nn) R^(6b) N209 R^(1b) R^(3n) R^(4c)R^(5nn) R^(6a) N210 R^(1b) R^(3o) R^(4c) R^(5nn) R^(6b) N211 R^(1b)R^(3o) R^(4c) R^(5nn) R^(6c) N212 R^(1b) R^(3p) R^(4e) R^(5nn) R^(6b)N213 R^(1b) R^(3p) R^(4e) R^(5nn) R^(6b) N214 R^(1b) R^(3q) R^(4e)R^(5nn) R^(6b) N215 R^(1b) R^(3q) R^(4e) R^(5nn) R^(6b) N216 R^(1b)R^(3r) R^(4e) R^(5nn) R^(6b) N217 R^(1b) R^(3r) R^(4e) R^(5nn) R^(6b)N218 R^(1b) R^(3n) R^(4c) R^(5oo) R^(6a) N219 R^(1b) R^(3o) R^(4c)R^(5oo) R^(6b) N220 R^(1b) R^(3o) R^(4c) R^(5oo) R^(6c) N221 R^(1b)R^(3p) R^(4e) R^(5oo) R^(6b) N222 R^(1b) R^(3p) R^(4e) R^(5oo) R^(6b)N223 R^(1b) R^(3q) R^(4e) R^(5oo) R^(6b) N224 R^(1b) R^(3q) R^(4e)R^(5oo) R^(6b) N225 R^(1b) R^(3r) R^(4e) R^(5oo) R^(6b) N226 R^(1b)R^(3r) R^(4e) R^(5oo) R^(6b) N227 R^(1b) R^(3n) R^(4c) R^(5pp) R^(6a)N228 R^(1b) R^(3o) R^(4c) R^(5qq) R^(6b) N229 R^(1b) R^(3o) R^(4c)R^(5qq) R^(6c) N230 R^(1b) R^(3p) R^(4e) R^(5qq) R^(6b) N231 R^(1b)R^(3p) R^(4e) R^(5qq) R^(6b) N232 R^(1b) R^(3q) R^(4e) R^(5qq) R^(6b)N233 R^(1b) R^(3q) R^(4e) R^(5qq) R^(6b) N234 R^(1b) R^(3r) R^(4e)R^(5qq) R^(6b) N235 R^(1b) R^(3r) R^(4e) R^(5qq) R^(6b) N236 R^(1b)R^(3n) R^(4c) R^(5pp) R^(6a) N237 R^(1b) R^(3o) R^(4c) R^(5qq) R^(6b)N238 R^(1b) R^(3o) R^(4c) R^(5qq) R^(6c) N239 R^(1b) R^(3p) R^(4e)R^(5qq) R^(6b) N240 R^(1b) R^(3p) R^(4e) R^(5qq) R^(6b) N241 R^(1b)R^(3q) R^(4e) R^(5qq) R^(6b) N242 R^(1b) R^(3q) R^(4e) R^(5qq) R^(6b)N243 R^(1b) R^(3r) R^(4e) R^(5qq) R^(6b) N244 R^(1b) R^(3r) R^(4e)R^(5qq) R^(6b) N245 R^(1b) R^(3n) R^(4c) R^(5rr) R^(6a) N246 R^(1b)R^(3o) R^(4c) R^(5rr) R^(6b) N247 R^(1b) R^(3o) R^(4c) R^(5rr) R^(6c)N248 R^(1b) R^(3p) R^(4e) R^(5rr) R^(6b) N249 R^(1b) R^(3p) R^(4e)R^(5rr) R^(6b) N250 R^(1b) R^(3q) R^(4e) R^(5rr) R^(6b) N251 R^(1b)R^(3q) R^(4e) R^(5rr) R^(6b) N252 R^(1b) R^(3r) R^(4e) R^(5rr) R^(6b)N253 R^(1b) R^(3r) R^(4e) R^(5rr) R^(6b) N254 R^(1b) R^(3s) R^(4a)R^(5ss) R^(6b) N255 R^(1b) R^(3t) R^(4b) R^(5ss) R^(6b) N256 R^(1b)R^(3g) R^(4e) R^(5ss) R^(6b) N257 R^(1b) R^(3h) R^(4e) R^(5ss) R^(6b)N258 R^(1b) R^(3s) R^(4a) R^(5tt) R^(6b) N259 R^(1b) R^(3t) R^(4b)R^(5tt) R^(6b) N260 R^(1b) R^(3g) R^(4e) R^(5tt) R^(6b) N261 R^(1b)R^(3h) R^(4e) R^(5tt) R^(6b) N262 R^(1b) R^(3s) R^(4a) R^(5uu) R^(6b)N263 R^(1b) R^(3t) R^(4b) R^(5uu) R^(6b) N264 R^(1b) R^(3g) R^(4e)R^(5uu) R^(6b) N265 R^(1b) R^(3h) R^(4e) R^(5uu) R^(6b) N266 R^(1b)R^(3s) R^(4a) R^(5vv) R^(6b) N267 R^(1b) R^(3t) R^(4b) R^(5vv) R^(6b)N268 R^(1b) R^(3g) R^(4e) R^(5vv) R^(6b) N269 R^(1b) R^(3h) R^(4e)R^(5vv) R^(6b) N270 R^(1b) R^(3s) R^(4a) R^(5ww) R^(6b) N271 R^(1b)R^(3t) R^(4b) R^(5ww) R^(6b) N272 R^(1b) R^(3g) R^(4e) R^(5ww) R^(6b)N273 R^(1b) R^(3h) R^(4e) R^(5ww) R^(6b) N274 R^(1b) R^(3s) R^(4a)R^(5xx) R^(6b) N275 R^(1b) R^(3t) R^(4b) R^(5xx) R^(6b) N276 R^(1b)R^(3g) R^(4e) R^(5xx) R^(6b) N277 R^(1b) R^(3h) R^(4e) R^(5xx) R^(6b)N278 R^(1b) R^(3s) R^(4a) R^(5zz) R^(6b) N279 R^(1b) R^(3t) R^(4b)R^(5zz) R^(6b) N280 R^(1b) R^(3g) R^(4e) R^(5zz) R^(6b) N281 R^(1b)R^(3h) R^(4e) R^(5zz) R^(6b) N282 R^(1b) R^(3s) R^(4a) R^(5ba) R^(6b)N283 R^(1b) R^(3t) R^(4b) R^(5ba) R^(6b) N284 R^(1b) R^(3g) R^(4e)R^(5ba) R^(6b) N285 R^(1b) R^(3h) R^(4e) R^(5ba) R^(6b) N286 R^(1b)R^(3s) R^(4a) R^(5bc) R^(6b) N287 R^(1b) R^(3t) R^(4b) R^(5bc) R^(6b)N288 R^(1b) R^(3g) R^(4e) R^(5bc) R^(6b) N289 R^(1b) R^(3h) R^(4e)R^(5bc) R^(6b) N290 R^(1b) R^(3s) R^(4a) R^(5bd) R^(6b) N291 R^(1b)R^(3t) R^(4b) R^(5bd) R^(6b) N292 R^(1b) R^(3g) R^(4e) R^(5bd) R^(6b)N293 R^(1b) R^(3h) R^(4e) R^(5bd) R^(6b) N294 R^(1b) R^(3s) R^(4a)R^(5be) R^(6b) N295 R^(1b) R^(3t) R^(4b) R^(5be) R^(6b) N296 R^(1b)R^(3g) R^(4e) R^(5be) R^(6b) N297 R^(1b) R^(3h) R^(4e) R^(5be) R^(6b)N298 R^(1b) R^(3s) R^(4a) R^(5bf) R^(6b) N299 R^(1b) R^(3t) R^(4b)R^(5bf) R^(6b) N300 R^(1b) R^(3g) R^(4e) R^(5bf) R^(6b) N301 R^(1b)R^(3h) R^(4e) R^(5bf) R^(6b) N302 R^(1b) R^(3s) R^(4a) R^(5bg) R^(6b)N303 R^(1b) R^(3t) R^(4b) R^(5bg) R^(6b) N304 R^(1b) R^(3g) R^(4e)R^(5bg) R^(6b) N305 R^(1b) R^(3h) R^(4e) R^(5bg) R^(6b) N306 R^(1b)R^(3s) R^(4a) R^(5bh) R^(6b) N307 R^(1b) R^(3t) R^(4b) R^(5bh) R^(6b)N308 R^(1b) R^(3g) R^(4e) R^(5bh) R^(6b) N309 R^(1b) R^(3h) R^(4e)R^(5bh) R^(6b) N310 R^(1b) R^(3s) R^(4a) R^(5bi) R^(6b) N311 R^(1b)R^(3t) R^(4b) R^(5bi) R^(6b) N312 R^(1b) R^(3g) R^(4e) R^(5bi) R^(6b)N313 R^(1b) R^(3h) R^(4e) R^(5bi) R^(6b) N314 R^(1b) R^(3s) R^(4a)R^(5bj) R^(6b) N315 R^(1b) R^(3t) R^(4b) R^(5bj) R^(6b) N316 R^(1b)R^(3g) R^(4e) R^(5bj) R^(6b) N317 R^(1b) R^(3h) R^(4e) R^(5bj) R^(6b)N318 R^(1b) R^(3s) R^(4a) R^(5bk) R^(6b) N319 R^(1b) R^(3t) R^(4b)R^(5bk) R^(6b) N320 R^(1b) R^(3g) R^(4e) R^(5bk) R^(6b) N321 R^(1b)R^(3h) R^(4e) R^(5bk) R^(6b) N322 R^(1b) R^(3s) R^(4a) R^(5bl) R^(6b)N323 R^(1b) R^(3t) R^(4b) R^(5bl) R^(6b) N324 R^(1b) R^(3g) R^(4e)R^(5bl) R^(6b) N325 R^(1b) R^(3h) R^(4e) R^(5bl) R^(6b) N326 R^(1b)R^(3s) R^(4a) R^(5bm) R^(6b) N327 R^(1b) R^(3t) R^(4b) R^(5bm) R^(6b)N328 R^(1b) R^(3g) R^(4e) R^(5bm) R^(6b) N329 R^(1b) R^(3h) R^(4e)R^(5bm) R^(6b) N330 R^(1b) R^(3s) R^(4a) R^(5bn) R^(6b) N331 R^(1b)R^(3t) R^(4b) R^(5bn) R^(6b) N332 R^(1b) R^(3g) R^(4e) R^(5bn) R^(6b)N333 R^(1b) R^(3h) R^(4e) R^(5bn) R^(6b) N334 R^(1b) R^(3s) R^(4a)R^(5bo) R^(6b) N335 R^(1b) R^(3t) R^(4b) R^(5bo) R^(6b) N336 R^(1b)R^(3g) R^(4e) R^(5bo) R^(6b) N337 R^(1b) R^(3h) R^(4e) R^(5bo) R^(6b)N338 R^(1b) R^(3s) R^(4a) R^(5bp) R^(6b) N339 R^(1b) R^(3t) R^(4b)R^(5bp) R^(6b) N340 R^(1b) R^(3g) R^(4e) R^(5bp) R^(6b) N341 R^(1b)R^(3h) R^(4e) R^(5bp) R^(6b) N342 R^(1b) R^(3s) R^(4a) R^(5bq) R^(6b)N343 R^(1b) R^(3t) R^(4b) R^(5bq) R^(6b) N344 R^(1b) R^(3g) R^(4e)R^(5bq) R^(6b) N345 R^(1b) R^(3h) R^(4e) R^(5bq) R^(6b) N346 R^(1b)R^(3s) R^(4a) R^(5br) R^(6b) N347 R^(1b) R^(3t) R^(4b) R^(5bq) R^(6b)N348 R^(1b) R^(3g) R^(4e) R^(5bq) R^(6b) N349 R^(1b) R^(3h) R^(4e)R^(5bq) R^(6b) N350 R^(1b) R^(3s) R^(4a) R^(5bs) R^(6b) N351 R^(1b)R^(3t) R^(4b) R^(5bs) R^(6b) N352 R^(1b) R^(3g) R^(4e) R^(5bs) R^(6b)N353 R^(1b) R^(3h) R^(4e) R^(5bs) R^(6b) N354 R^(1b) R^(3s) R^(4a)R^(5bt) R^(6b) N355 R^(1b) R^(3t) R^(4b) R^(5bt) R^(6b) N356 R^(1b)R^(3g) R^(4e) R^(5bt) R^(6b) N357 R^(1b) R^(3h) R^(4e) R^(5bt) R^(6b)N358 R^(1b) R^(3s) R^(4a) R^(5bu) R^(6b) N359 R^(1b) R^(3t) R^(4b)R^(5bu) R^(6b) N360 R^(1b) R^(3g) R^(4e) R^(5bu) R^(6b) N361 R^(1b)R^(3h) R^(4e) R^(5bu) R^(6b) N362 R^(1b) R^(3s) R^(4a) R^(5bv) R^(6b)N363 R^(1b) R^(3t) R^(4b) R^(5bv) R^(6b) N364 R^(1b) R^(3g) R^(4e)R^(5bv) R^(6b) N365 R^(1b) R^(3h) R^(4e) R^(5bv) R^(6b) N366 R^(1b)R^(3s) R^(4a) R^(5bw) R^(6b) N367 R^(1b) R^(3t) R^(4b) R^(5bw) R^(6b)N368 R^(1b) R^(3g) R^(4e) R^(5bw) R^(6b) N369 R^(1b) R^(3h) R^(4e)R^(5bw) R^(6b) N370 R^(1b) R^(3s) R^(4a) R^(5bx) R^(6b) N371 R^(1b)R^(3t) R^(4b) R^(5bx) R^(6b) N372 R^(1b) R^(3g) R^(4e) R^(5bx) R^(6b)N373 R^(1b) R^(3h) R^(4e) R^(5bx) R^(6b) N374 R^(1b) R^(3s) R^(4a)R^(5by) R^(6b) N375 R^(1b) R^(3t) R^(4b) R^(5by) R^(6b) N376 R^(1b)R^(3g) R^(4e) R^(5by) R^(6b) N377 R^(1b) R^(3h) R^(4e) R^(5by) R^(6b)N378 R^(1b) R^(3s) R^(4a) R^(5bz) R^(6b) N379 R^(1b) R^(3t) R^(4b)R^(5bz) R^(6b) N380 R^(1b) R^(3g) R^(4e) R^(5bz) R^(6b) N381 R^(1b)R^(3h) R^(4e) R^(5bz) R^(6b) N382 R^(1b) R^(3s) R^(4a) R^(5ca) R^(6b)N383 R^(1b) R^(3t) R^(4b) R^(5ca) R^(6b) N384 R^(1b) R^(3g) R^(4e)R^(5ca) R^(6b) N385 R^(1b) R^(3h) R^(4e) R^(5ca) R^(6b) N386 R^(1b)R^(3s) R^(4a) R^(5cb) R^(6b) N387 R^(1b) R^(3t) R^(4b) R^(5cb) R^(6b)N388 R^(1b) R^(3g) R^(4e) R^(5cb) R^(6b) N389 R^(1b) R^(3h) R^(4e)R^(5cb) R^(6b) N390 R^(1b) R^(3s) R^(4a) R^(5cd) R^(6b) N391 R^(1b)R^(3t) R^(4b) R^(5cd) R^(6b) N392 R^(1b) R^(3g) R^(4e) R^(5cd) R^(6b)N393 R^(1b) R^(3h) R^(4e) R^(5cd) R^(6b) N394 R^(1b) R^(3s) R^(4a)R^(5ce) R^(6b) N395 R^(1b) R^(3t) R^(4b) R^(5ce) R^(6b) N396 R^(1b)R^(3g) R^(4e) R^(5ce) R^(6b) N397 R^(1b) R^(3h) R^(4e) R^(5ce) R^(6b)N398 R^(1b) R^(3s) R^(4a) R^(5cf) R^(6b) N399 R^(1b) R^(3t) R^(4b)R^(5cf) R^(6b) N400 R^(1b) R^(3g) R^(4e) R^(5cf) R^(6b) N401 R^(1b)R^(3h) R^(4e) R^(5cf) R^(6b) N402 R^(1b) R^(3s) R^(4a) R^(5cg) R^(6b)N403 R^(1b) R^(3t) R^(4b) R^(5cg) R^(6b) N404 R^(1b) R^(3g) R^(4e)R^(5cg) R^(6b) N405 R^(1b) R^(3h) R^(4e) R^(5cg) R^(6b) N406 R^(1b)R^(3s) R^(4a) R^(5ch) R^(6b) N407 R^(1b) R^(3t) R^(4b) R^(5ch) R^(6b)N408 R^(1b) R^(3g) R^(4e) R^(5ch) R^(6b) N409 R^(1b) R^(3h) R^(4e)R^(5ch) R^(6b) N410 R^(1b) R^(3s) R^(4a) R^(5ci) R^(6b) N411 R^(1b)R^(3t) R^(4b) R^(5ci) R^(6b) N412 R^(1b) R^(3g) R^(4e) R^(5ci) R^(6b)N413 R^(1b) R^(3h) R^(4e) R^(5ci) R^(6b) N414 R^(1b) R^(3s) R^(4a)R^(5cj) R^(6b) N415 R^(1b) R^(3t) R^(4b) R^(5cj) R^(6b) N416 R^(1b)R^(3g) R^(4e) R^(5cj) R^(6b) N417 R^(1b) R^(3h) R^(4e) R^(5cj) R^(6b)N418 R^(1b) R^(3s) R^(4a) R^(5ck) R^(6b) N419 R^(1b) R^(3t) R^(4b)R^(5ck) R^(6b) N420 R^(1b) R^(3g) R^(4e) R^(5ck) R^(6b) N421 R^(1b)R^(3h) R^(4e) R^(5ck) R^(6b) N422 R^(1b) R^(3s) R^(4a) R^(5cl) R^(6b)N423 R^(1b) R^(3t) R^(4b) R^(5cl) R^(6b) N424 R^(1b) R^(3g) R^(4e)R^(5cl) R^(6b) N425 R^(1b) R^(3h) R^(4e) R^(5cl) R^(6b) N426 R^(1b)R^(3s) R^(4a) R^(5cm) R^(6b) N427 R^(1b) R^(3t) R^(4b) R^(5cm) R^(6b)N428 R^(1b) R^(3g) R^(4e) R^(5cm) R^(6b) N429 R^(1b) R^(3h) R^(4e)R^(5cm) R^(6b) N430 R^(1b) R^(3s) R^(4a) R^(5cn) R^(6b) N431 R^(1b)R^(3t) R^(4b) R^(5cn) R^(6b) N432 R^(1b) R^(3g) R^(4e) R^(5cn) R^(6b)N433 R^(1b) R^(3h) R^(4e) R^(5cn) R^(6b) N434 R^(1b) R^(3s) R^(4a)R^(5co) R^(6b) N435 R^(1b) R^(3t) R^(4b) R^(5co) R^(6b) N436 R^(1b)R^(3g) R^(4e) R^(5co) R^(6b) N437 R^(1b) R^(3h) R^(4e) R^(5co) R^(6b)N438 R^(1b) R^(3s) R^(4a) R^(5cp) R^(6b) N439 R^(1b) R^(3t) R^(4b)R^(5cp) R^(6b) N440 R^(1b) R^(3g) R^(4e) R^(5cp) R^(6b) N441 R^(1b)R^(3h) R^(4e) R^(5cp) R^(6b) N442 R^(1b) R^(3s) R^(4a) R^(5cq) R^(6b)N443 R^(1b) R^(3t) R^(4b) R^(5cq) R^(6b) N444 R^(1b) R^(3g) R^(4e)R^(5cq) R^(6b) N445 R^(1b) R^(3h) R^(4e) R^(5cq) R^(6b) N446 R^(1b)R^(3s) R^(4a) R^(5cr) R^(6b) N447 R^(1b) R^(3t) R^(4b) R^(5cr) R^(6b)N448 R^(1b) R^(3g) R^(4e) R^(5cr) R^(6b) N449 R^(1b) R^(3h) R^(4e)R^(5cr) R^(6b) N450 R^(1b) R^(3s) R^(4a) R^(5cs) R^(6b) N451 R^(1b)R^(3t) R^(4b) R^(5cs) R^(6b) N452 R^(1b) R^(3g) R^(4e) R^(5cs) R^(6b)N453 R^(1b) R^(3h) R^(4e) R^(5cs) R^(6b) N454 R^(1b) R^(3s) R^(4a)R^(5ct) R^(6b) N455 R^(1b) R^(3t) R^(4b) R^(5ct) R^(6b) N456 R^(1b)R^(3g) R^(4e) R^(5ct) R^(6b) N457 R^(1b) R^(3h) R^(4e) R^(5ct) R^(6b)N458 R^(1b) R^(3s) R^(4a) R^(5cu) R^(6b) N459 R^(1b) R^(3t) R^(4b)R^(5cu) R^(6b) N460 R^(1b) R^(3g) R^(4e) R^(5cu) R^(6b) N461 R^(1b)R^(3h) R^(4e) R^(5cu) R^(6b) N462 R^(1b) R^(3s) R^(4a) R^(5cv) R^(6b)N463 R^(1b) R^(3t) R^(4b) R^(5cv) R^(6b) N464 R^(1b) R^(3g) R^(4e)R^(5cv) R^(6b) N465 R^(1b) R^(3h) R^(4e) R^(5cv) R^(6b) N466 R^(1b)R^(3s) R^(4a) R^(5cw) R^(6b) N467 R^(1b) R^(3t) R^(4b) R^(5cw) R^(6b)N468 R^(1b) R^(3g) R^(4e) R^(5cw) R^(6b) N469 R^(1b) R^(3h) R^(4e)R^(5cw) R^(6b) N470 R^(1b) R^(3s) R^(4a) R^(5cx) R^(6b) N471 R^(1b)R^(3t) R^(4b) R^(5cx) R^(6b) N472 R^(1b) R^(3g) R^(4e) R^(5cx) R^(6b)N473 R^(1b) R^(3h) R^(4e) R^(5cx) R^(6b) N474 R^(1b) R^(3s) R^(4a)R^(5cy) R^(6b) N475 R^(1b) R^(3t) R^(4b) R^(5cy) R^(6b) N476 R^(1b)R^(3g) R^(4e) R^(5cy) R^(6b) N477 R^(1b) R^(3h) R^(4e) R^(5cy) R^(6b)N478 R^(1b) R^(3s) R^(4a) R^(5cz) R^(6b) N479 R^(1b) R^(3t) R^(4b)R^(5cz) R^(6b) N480 R^(1b) R^(3g) R^(4e) R^(5cz) R^(6b) N481 R^(1b)R^(3h) R^(4e) R^(5cz) R^(6b) N482 R^(1b) R^(3s) R^(4a) R^(5da) R^(6b)N483 R^(1b) R^(3t) R^(4b) R^(5da) R^(6b) N484 R^(1b) R^(3g) R^(4e)R^(5da) R^(6b) N485 R^(1b) R^(3h) R^(4e) R^(5da) R^(6b) N486 R^(1b)R^(3s) R^(4a) R^(5db) R^(6b) N487 R^(1b) R^(3t) R^(4b) R^(5db) R^(6b)N488 R^(1b) R^(3g) R^(4e) R^(5db) R^(6b) N489 R^(1b) R^(3h) R^(4e)R^(5db) R^(6b) N490 R^(1b) R^(3s) R^(4a) R^(5dc) R^(6b) N491 R^(1b)R^(3t) R^(4b) R^(5dc) R^(6b) N492 R^(1b) R^(3g) R^(4e) R^(5dc) R^(6b)N493 R^(1b) R^(3h) R^(4e) R^(5dc) R^(6b) N494 R^(1b) R^(3s) R^(4a)R^(5de) R^(6b) N495 R^(1b) R^(3t) R^(4b) R^(5de) R^(6b) N496 R^(1b)R^(3g) R^(4e) R^(5de) R^(6b) N497 R^(1b) R^(3h) R^(4e) R^(5de) R^(6b)N498 R^(1b) R^(3s) R^(4a) R^(5df) R^(6b) N499 R^(1b) R^(3t) R^(4b)R^(5df) R^(6b) N500 R^(1b) R^(3g) R^(4e) R^(5df) R^(6b) N501 R^(1b)R^(3h) R^(4e) R^(5df) R^(6b) N502 R^(1b) R^(3s) R^(4a) R^(5dg) R^(6b)N503 R^(1b) R^(3t) R^(4b) R^(5dg) R^(6b) N504 R^(1b) R^(3g) R^(4e)R^(5dg) R^(6b) N505 R^(1b) R^(3h) R^(4e) R^(5dg) R^(6b) N506 R^(1b)R^(3s) R^(4a) R^(5dh) R^(6b) N507 R^(1b) R^(3t) R^(4b) R^(5dh) R^(6b)N508 R^(1b) R^(3g) R^(4e) R^(5dh) R^(6b) N509 R^(1b) R^(3h) R^(4e)R^(5dh) R^(6b) N510 R^(1b) R^(3s) R^(4a) R^(5di) R^(6b) N511 R^(1b)R^(3t) R^(4b) R^(5di) R^(6b) N512 R^(1b) R^(3g) R^(4e) R^(5di) R^(6b)N513 R^(1b) R^(3h) R^(4e) R^(5di) R^(6b) N514 R^(1b) R^(3s) R^(4a)R^(5dj) R^(6b) N515 R^(1b) R^(3t) R^(4b) R^(5dj) R^(6b) N516 R^(1b)R^(3g) R^(4e) R^(5dj) R^(6b) N517 R^(1b) R^(3h) R^(4e) R^(5dj) R^(6b)N518 R^(1b) R^(3s) R^(4a) R^(5dk) R^(6b) N519 R^(1b) R^(3t) R^(4b)R^(5dk) R^(6b) N520 R^(1b) R^(3g) R^(4e) R^(5dk) R^(6b) N521 R^(1b)R^(3h) R^(4e) R^(5dk) R^(6b) N522 R^(1b) R^(3s) R^(4a) R^(5dl) R^(6b)N523 R^(1b) R^(3t) R^(4b) R^(5dl) R^(6b) N524 R^(1b) R^(3g) R^(4e)R^(5dl) R^(6b) N525 R^(1b) R^(3h) R^(4e) R^(5dl) R^(6b) N526 R^(1b)R^(3s) R^(4a) R^(5dm) R^(6b) N527 R^(1b) R^(3t) R^(4b) R^(5dm) R^(6b)N528 R^(1b) R^(3g) R^(4e) R^(5dm) R^(6b) N529 R^(1b) R^(3h) R^(4e)R^(5dm) R^(6b) N530 R^(1b) R^(3s) R^(4a) R^(5dn) R^(6b) N531 R^(1b)R^(3t) R^(4b) R^(5dn) R^(6b) N532 R^(1b) R^(3g) R^(4e) R^(5dn) R^(6b)N533 R^(1b) R^(3h) R^(4e) R^(5dn) R^(6b) N534 R^(1b) R^(3s) R^(4a)R^(5do) R^(6b) N535 R^(1b) R^(3t) R^(4b) R^(5do) R^(6b) N536 R^(1b)R^(3g) R^(4e) R^(5do) R^(6b) N537 R^(1b) R^(3h) R^(4e) R^(5do) R^(6b)N538 R^(1b) R^(3s) R^(4a) R^(5dp) R^(6b) N539 R^(1b) R^(3t) R^(4b)R^(5dp) R^(6b) N540 R^(1b) R^(3g) R^(4e) R^(5dp) R^(6b) N541 R^(1b)R^(3h) R^(4e) R^(5dp) R^(6b) N542 R^(1b) R^(3s) R^(4a) R^(5dq) R^(6b)N543 R^(1b) R^(3t) R^(4b) R^(5dq) R^(6b) N544 R^(1b) R^(3g) R^(4e)R^(5dq) R^(6b) N545 R^(1b) R^(3h) R^(4e) R^(5dq) R^(6b) N546 R^(1b)R^(3s) R^(4a) R^(5dr) R^(6b) N547 R^(1b) R^(3t) R^(4b) R^(5dr) R^(6b)N548 R^(1b) R^(3g) R^(4e) R^(5dr) R^(6b) N549 R^(1b) R^(3h) R^(4e)R^(5dr) R^(6b) N550 R^(1b) R^(3s) R^(4a) R^(5ds) R^(6b) N551 R^(1b)R^(3t) R^(4b) R^(5ds) R^(6b) N552 R^(1b) R^(3g) R^(4e) R^(5ds) R^(6b)N553 R^(1b) R^(3h) R^(4e) R^(5ds) R^(6b) N554 R^(1b) R^(3s) R^(4a)R^(5dt) R^(6b) N555 R^(1b) R^(3t) R^(4b) R^(5dt) R^(6b) N556 R^(1b)R^(3g) R^(4e) R^(5dt) R^(6b) N557 R^(1b) R^(3h) R^(4e) R^(5dt) R^(6b)N558 R^(1b) R^(3s) R^(4a) R^(5du) R^(6b) N559 R^(1b) R^(3t) R^(4b)R^(5du) R^(6b) N560 R^(1b) R^(3g) R^(4e) R^(5du) R^(6b) N561 R^(1b)R^(3h) R^(4e) R^(5du) R^(6b) N562 R^(1b) R^(3s) R^(4a) R^(5dv) R^(6b)N563 R^(1b) R^(3t) R^(4b) R^(5dv) R^(6b) N564 R^(1b) R^(3g) R^(4e)R^(5dv) R^(6b) N565 R^(1b) R^(3h) R^(4e) R^(5dv) R^(6b) N566 R^(1b)R^(3s) R^(4a) R^(5dw) R^(6b) N567 R^(1b) R^(3t) R^(4b) R^(5dw) R^(6b)N568 R^(1b) R^(3g) R^(4e) R^(5dw) R^(6b) N569 R^(1b) R^(3h) R^(4e)R^(5dw) R^(6b) N570 R^(1b) R^(3s) R^(4a) R^(5dx) R^(6b) N571 R^(1b)R^(3t) R^(4b) R^(5dx) R^(6b) N572 R^(1b) R^(3g) R^(4e) R^(5dx) R^(6b)N573 R^(1b) R^(3h) R^(4e) R^(5dx) R^(6b) N574 R^(1b) R^(3s) R^(4a)R^(5ea) R^(6b) N575 R^(1b) R^(3t) R^(4b) R^(5ea) R^(6b) N576 R^(1b)R^(3g) R^(4e) R^(5ea) R^(6b) N577 R^(1b) R^(3h) R^(4e) R^(5ea) R^(6b)N578 R^(1b) R^(3s) R^(4a) R^(5eb) R^(6b) N579 R^(1b) R^(3t) R^(4b)R^(5eb) R^(6b) N580 R^(1b) R^(3g) R^(4e) R^(5eb) R^(6b) N581 R^(1b)R^(3h) R^(4e) R^(5eb) R^(6b) N582 R^(1b) R^(3s) R^(4a) R^(5ec) R^(6b)N583 R^(1b) R^(3t) R^(4b) R^(5ec) R^(6b) N584 R^(1b) R^(3g) R^(4e)R^(5ec) R^(6b) N585 R^(1b) R^(3h) R^(4e) R^(5ec) R^(6b) N586 R^(1b)R^(3s) R^(4a) R^(5ed) R^(6b) N587 R^(1b) R^(3t) R^(4b) R^(5ed) R^(6b)N588 R^(1b) R^(3g) R^(4e) R^(5ed) R^(6b) N589 R^(1b) R^(3h) R^(4e)R^(5ed) R^(6b) N590 R^(1b) R^(3s) R^(4a) R^(5ef) R^(6b) N591 R^(1b)R^(3t) R^(4b) R^(5ef) R^(6b) N592 R^(1b) R^(3g) R^(4e) R^(5ef) R^(6b)N593 R^(1b) R^(3h) R^(4e) R^(5ef) R^(6b) N594 R^(1b) R^(3s) R^(4a)R^(5eg) R^(6b) N595 R^(1b) R^(3t) R^(4b) R^(5eg) R^(6b) N596 R^(1b)R^(3g) R^(4e) R^(5eg) R^(6b) N597 R^(1b) R^(3h) R^(4e) R^(5eg) R^(6b)N598 R^(1b) R^(3s) R^(4a) R^(5eh) R^(6b) N599 R^(1b) R^(3t) R^(4b)R^(5eh) R^(6b) N600 R^(1b) R^(3g) R^(4e) R^(5eh) R^(6b) N601 R^(1b)R^(3h) R^(4e) R^(5eh) R^(6b) N602 R^(1b) R^(3s) R^(4a) R^(5ei) R^(6b)N603 R^(1b) R^(3t) R^(4b) R^(5ei) R^(6b) N604 R^(1b) R^(3g) R^(4e)R^(5ei) R^(6b) N605 R^(1b) R^(3h) R^(4e) R^(5ei) R^(6b) N606 R^(1b)R^(3s) R^(4a) R^(5ej) R^(6b) N607 R^(1b) R^(3t) R^(4b) R^(5ej) R^(6b)N608 R^(1b) R^(3g) R^(4e) R^(5ej) R^(6b) N609 R^(1b) R^(3h) R^(4e)R^(5ej) R^(6b) N610 R^(1b) R^(3s) R^(4a) R^(5ek) R^(6b) N611 R^(1b)R^(3t) R^(4b) R^(5ej) R^(6b) N612 R^(1b) R^(3g) R^(4e) R^(5ej) R^(6b)N613 R^(1b) R^(3h) R^(4e) R^(5ej) R^(6b) N614 R^(1b) R^(3s) R^(4a)R^(5el) R^(6b) N615 R^(1b) R^(3t) R^(4b) R^(5el) R^(6b) N616 R^(1b)R^(3g) R^(4e) R^(5el) R^(6b) N617 R^(1b) R^(3h) R^(4e) R^(5el) R^(6b)N618 R^(1b) R^(3s) R^(4a) R^(5em) R^(6b) N619 R^(1b) R^(3t) R^(4b)R^(5em) R^(6b) N620 R^(1b) R^(3g) R^(4e) R^(5em) R^(6b) N621 R^(1b)R^(3h) R^(4e) R^(5em) R^(6b) N622 R^(1b) R^(3s) R^(4a) R^(5en) R^(6b)N623 R^(1b) R^(3t) R^(4b) R^(5en) R^(6b) N624 R^(1b) R^(3g) R^(4e)R^(5en) R^(6b) N625 R^(1b) R^(3h) R^(4e) R^(5en) R^(6b) N626 R^(1b)R^(3s) R^(4a) R^(5eo) R^(6b) N627 R^(1b) R^(3t) R^(4b) R^(5eo) R^(6b)N628 R^(1b) R^(3g) R^(4e) R^(5eo) R^(6b) N629 R^(1b) R^(3h) R^(4e)R^(5eo) R^(6b) N630 R^(1b) R^(3s) R^(4a) R^(5ep) R^(6b) N631 R^(1b)R^(3t) R^(4b) R^(5ep) R^(6b) N632 R^(1b) R^(3g) R^(4e) R^(5ep) R^(6b)N633 R^(1b) R^(3h) R^(4e) R^(5ep) R^(6b) N634 R^(1b) R^(3s) R^(4a)R^(5eq) R^(6b) N635 R^(1b) R^(3t) R^(4b) R^(5eq) R^(6b) N636 R^(1b)R^(3g) R^(4e) R^(5eq) R^(6b) N637 R^(1b) R^(3h) R^(4e) R^(5eq) R^(6b)N638 R^(1b) R^(3s) R^(4a) R^(5er) R^(6b) N639 R^(1b) R^(3t) R^(4b)R^(ber) R^(6b) N640 R^(1b) R^(3g) R^(4e) R^(ber) R^(6b) N641 R^(1b)R^(3h) R^(4e) R^(ber) R^(6b) N642 R^(1b) R^(3s) R^(4a) R^(5es) R^(6b)N643 R^(1b) R^(3t) R^(4b) R^(5es) R^(6b) N644 R^(1b) R^(3g) R^(4e)R^(5es) R^(6b) N645 R^(1b) R^(3h) R^(4e) R^(5es) R^(6b) N646 R^(1b)R^(3s) R^(4a) R^(bet) R^(6b) N647 R^(1b) R^(3t) R^(4b) R^(bet) R^(6b)N648 R^(1b) R^(3g) R^(4e) R^(bet) R^(6b) N649 R^(1b) R^(3h) R^(4e)R^(bet) R^(6b) N650 R^(1b) R^(3s) R^(4a) R^(5eu) R^(6b) N651 R^(1b)R^(3t) R^(4b) R^(5eu) R^(6b) N652 R^(1b) R^(3g) R^(4e) R^(5eu) R^(6b)N653 R^(1b) R^(3h) R^(4e) R^(5eu) R^(6b) N654 R^(1b) R^(3s) R^(4a)R^(5ev) R^(6b) N655 R^(1b) R^(3t) R^(4b) R^(5ev) R^(6b) N656 R^(1b)R^(3g) R^(4e) R^(5ev) R^(6b) N657 R^(1b) R^(3h) R^(4e) R^(5ev) R^(6b)N658 R^(1b) R^(3s) R^(4a) R^(5ex) R^(6b) N659 R^(1b) R^(3t) R^(4b)R^(5ex) R^(6b) N660 R^(1b) R^(3g) R^(4e) R^(5ex) R^(6b) N661 R^(1b)R^(3h) R^(4e) R^(5ex) R^(6b) N662 R^(1b) R^(3s) R^(4a) R^(5ey) R^(6b)N663 R^(1b) R^(3t) R^(4b) R^(5ey) R^(6b) N664 R^(1b) R^(3g) R^(4e)R^(5ey) R^(6b) N665 R^(1b) R^(3h) R^(4e) R^(5ey) R^(6b) N666 R^(1b)R^(3s) R^(4a) R^(5ez) R^(6b) N667 R^(1b) R^(3t) R^(4b) R^(5ez) R^(6b)N668 R^(1b) R^(3g) R^(4e) R^(5ez) R^(6b) N669 R^(1b) R^(3h) R^(4e)R^(5ez) R^(6b) N670 R^(1b) R^(3s) R^(4a) R^(5fa) R^(6b) N671 R^(1b)R^(3t) R^(4b) R^(5fa) R^(6b) N672 R^(1b) R^(3g) R^(4e) R^(5fa) R^(6b)N673 R^(1b) R^(3h) R^(4e) R^(5fa) R^(6b) N674 R^(1b) R^(3s) R^(4a)R^(5fb) R^(6b) N675 R^(1b) R^(3t) R^(4b) R^(5fb) R^(6b) N676 R^(1b)R^(3g) R^(4e) R^(5fb) R^(6b) N677 R^(1b) R^(3h) R^(4e) R^(5fb) R^(6b)N678 R^(1b) R^(3s) R^(4a) R^(5fc) R^(6b) N679 R^(1b) R^(3t) R^(4b)R^(5fc) R^(6b) N680 R^(1b) R^(3g) R^(4e) R^(5fc) R^(6b) N681 R^(1b)R^(3h) R^(4e) R^(5fc) R^(6b) N682 R^(1b) R^(3s) R^(4a) R^(5fd) R^(6b)N683 R^(1b) R^(3t) R^(4b) R^(5fd) R^(6b) N684 R^(1b) R^(3g) R^(4e)R^(5fd) R^(6b) N685 R^(1b) R^(3h) R^(4e) R^(5fd) R^(6b) N686 R^(1b)R^(3s) R^(4a) R^(5fe) R^(6b) N687 R^(1b) R^(3t) R^(4b) R^(5fe) R^(6b)N688 R^(1b) R^(3g) R^(4e) R^(5fe) R^(6b) N689 R^(1b) R^(3h) R^(4e)R^(5fe) R^(6b) N690 R^(1b) R^(3s) R^(4a) R^(5fg) R^(6b) N691 R^(1b)R^(3t) R^(4b) R^(5fg) R^(6b) N692 R^(1b) R^(3g) R^(4e) R^(5fg) R^(6b)N693 R^(1b) R^(3h) R^(4e) R^(5fg) R^(6b) N694 R^(1b) R^(3s) R^(4a)R^(5fh) R^(6b) N695 R^(1b) R^(3t) R^(4b) R^(5fh) R^(6b) N696 R^(1b)R^(3g) R^(4e) R^(5fh) R^(6b) N697 R^(1b) R^(3h) R^(4e) R^(5fh) R^(6b)N698 R^(1b) R^(3s) R^(4a) R^(5fi) R^(6b) N699 R^(1b) R^(3t) R^(4b)R^(5fi) R^(6b) N700 R^(1b) R^(3g) R^(4e) R^(5fi) R^(6b) N701 R^(1b)R^(3h) R^(4e) R^(5fi) R^(6b) N702 R^(1b) R^(3s) R^(4a) R^(5fj) R^(6b)N703 R^(1b) R^(3t) R^(4b) R^(5fj) R^(6b) N704 R^(1b) R^(3g) R^(4e)R^(5fj) R^(6b) N705 R^(1b) R^(3h) R^(4e) R^(5fj) R^(6b) N706 R^(1b)R^(3s) R^(4a) R^(5fk) R^(6b) N707 R^(1b) R^(3t) R^(4b) R^(5fk) R^(6b)N708 R^(1b) R^(3g) R^(4e) R^(5fk) R^(6b) N709 R^(1b) R^(3h) R^(4e)R^(5fk) R^(6b) N710 R^(1b) R^(3s) R^(4a) R^(5fl) R^(6b) N711 R^(1b)R^(3t) R^(4b) R^(5fl) R^(6b) N712 R^(1b) R^(3g) R^(4e) R^(5fl) R^(6b)N713 R^(1b) R^(3h) R^(4e) R^(5fl) R^(6b) N714 R^(1b) R^(3s) R^(4a)R^(5fm) R^(6b) N715 R^(1b) R^(3t) R^(4b) R^(5fm) R^(6b) N716 R^(1b)R^(3g) R^(4e) R^(5fm) R^(6b) N717 R^(1b) R^(3h) R^(4e) R^(5fm) R^(6b)N718 R^(1b) R^(3s) R^(4a) R^(5fn) R^(6b) N719 R^(1b) R^(3t) R^(4b)R^(5fn) R^(6b) N720 R^(1b) R^(3g) R^(4e) R^(5fn) R^(6b) N721 R^(1b)R^(3h) R^(4e) R^(5fn) R^(6b) N722 R^(1b) R^(3s) R^(4a) R^(5fo) R^(6b)N723 R^(1b) R^(3t) R^(4b) R^(5fo) R^(6b) N724 R^(1b) R^(3g) R^(4e)R^(5fo) R^(6b) N725 R^(1b) R^(3h) R^(4e) R^(5fo) R^(6b) N726 R^(1b)R^(3s) R^(4a) R^(5fp) R^(6b) N727 R^(1b) R^(3t) R^(4b) R^(5fp) R^(6b)N728 R^(1b) R^(3g) R^(4e) R^(5fp) R^(6b) N729 R^(1b) R^(3h) R^(4e)R^(5fp) R^(6b) N730 R^(1b) R^(3s) R^(4a) R^(5fq) R^(6b) N731 R^(1b)R^(3t) R^(4b) R^(5fq) R^(6b) N732 R^(1b) R^(3g) R^(4e) R^(5fq) R^(6b)N733 R^(1b) R^(3h) R^(4e) R^(5fq) R^(6b) N734 R^(1b) R^(3s) R^(4a)R^(5fr) R^(6b) N735 R^(1b) R^(3t) R^(4b) R^(5fr) R^(6b) N736 R^(1b)R^(3g) R^(4e) R^(5fr) R^(6b) N737 R^(1b) R^(3h) R^(4e) R^(5fr) R^(6b)N738 R^(1b) R^(3s) R^(4a) R^(5fs) R^(6b) N739 R^(1b) R^(3t) R^(4b)R^(5fs) R^(6b) N740 R^(1b) R^(3g) R^(4e) R^(5fs) R^(6b) N741 R^(1b)R^(3h) R^(4e) R^(5fs) R^(6b) N742 R^(1b) R^(3s) R^(4a) R^(5ft) R^(6b)N743 R^(1b) R^(3t) R^(4b) R^(5ft) R^(6b) N744 R^(1b) R^(3g) R^(4e)R^(5ft) R^(6b) N745 R^(1b) R^(3h) R^(4e) R^(5ft) R^(6b) N746 R^(1b)R^(3s) R^(4a) R^(5fu) R^(6b) N747 R^(1b) R^(3t) R^(4b) R^(5fu) R^(6b)N748 R^(1b) R^(3g) R^(4e) R^(5fu) R^(6b) N749 R^(1b) R^(3h) R^(4e)R^(5fu) R^(6b) N750 R^(1b) R^(3s) R^(4a) R^(5fv) R^(6b) N751 R^(1b)R^(3t) R^(4b) R^(5fv) R^(6b) N752 R^(1b) R^(3g) R^(4e) R^(5fv) R^(6b)N753 R^(1b) R^(3h) R^(4e) R^(5fv) R^(6b) N754 R^(1b) R^(3s) R^(4a)R^(5fw) R^(6b) N755 R^(1b) R^(3t) R^(4b) R^(5fw) R^(6b) N756 R^(1b)R^(3g) R^(4e) R^(5fw) R^(6b) N757 R^(1b) R^(3h) R^(4e) R^(5fw) R^(6b)

Compounds of formula I as well as intermediates and reagents used can beprepared by the methods herein and as described in WO2008/101682 as wellas further methods known to a skilled chemist in a variety of ways, orthey are commercially available.

In a further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Chlorothalonil. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Fludioxonil. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Cyprodinil. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Fenpropidin. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Mandipropamid. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Fluazinam. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Procymedone. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Carbendazim. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Abamectin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Clothianidin. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Emamectin benzoate. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Imidacloprid. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Tefluthrin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Mefenoxam. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Orocymedone. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Thiamethoxam. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Lambda-cyhalothrin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Gamma-cyhalothrin.In a further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Profenofos. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Lufenuron. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Diflubenzuron. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Cypermethrin. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Novaluron. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Bifenthrin. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Methomyl. In a further preferred embodiment the componentA is a specific compound selected from Tables 1 to 164, a specificcompound selected from P.1 to P.372 or a specific compound selected fromQ.001 to Q.454 and the component B is Chlopyrifos. In a furtherpreferred embodiment the component A is a specific compound selectedfrom Tables 1 to 164, a specific compound selected from P.1 to P.372 ora specific compound selected from Q.001 to Q.454 and the component B isMethamidophos. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Endosulfan. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isBetacyfluthrin. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Triflumuron. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isTeflubenzuron. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Acephat. In a further preferred embodimentthe component A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Glyphosate. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Glufosinate. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Mesotrione. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Bicyclopyrone. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Tembotrione. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Sulcotrione. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is 2,4-D. In a furtherpreferred embodiment the component A is a specific compound selectedfrom Tables 1 to 164 or a specific compound selected from P.1 to P.372or a specific compound selected from Q.001 to Q.454 and the component Bis MCPA. In a further preferred embodiment the component A is a specificcompound selected from Tables 1 to 164, a specific compound selectedfrom P.1 to P.372 or a specific compound selected from Q.001 to Q.454and the component B is Trinexapac-ethyl. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isProhexadione-Ca. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Paclobutrazol. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isAcibenzolar-5-methyl. In a further preferred embodiment the component Ais a specific compound selected from Tables 1 to 164, a specificcompound selected from P.1 to P.372 or a specific compound selected fromQ.001 to Q.454 and the component B is Methyl-Jasmonate. In a furtherpreferred embodiment the component A is a specific compound selectedfrom Tables 1 to 164, a specific compound selected from P.1 to P.372 ora specific compound selected from Q.001 to Q.454 and the component B isCis-Jasmone. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Manganese. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isCyflufenamid. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Tebufloquin. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B is Copper. Ina further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Coumoxystrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Dicloaminostrobin.In a further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Flufenoxystrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Pyrametostrobin. Ina further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Pyraoxystrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Trifloxystrobin. Ina further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Azoxystrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Pyraclostrobin. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Picoxystrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Jiaxiangjunzhi. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Enoxastrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Triclopyricarb. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Fluoxastrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Dimoxystrobin. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Fenaminostrobin. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is the compound offormula II. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Cyproconazole. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isDifenoconazole. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Metconazole. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isPropiconazole. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Epoxiconazole. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isTebuconazole. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Flutriafol. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B is Ipconazole.In a further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is1-(2-chlorophenyl)-2-(1-chlorocycloprop-1-yl)-3-(1,2,4-triazol-1-yl)propan-2-ol[CAS number 120983-64-4]. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is prothioconazole. Ina further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is(S)-[3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol[CAS number 1229606-46-5]. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164 or aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol[CAS number 1229605-96-2]. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Pyrisoxazole. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-Pyrazole-4-carboxamide[CAS number 1228284-64-7]. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B isN-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide[CAS number 1072957-71-1]. In a further preferred embodiment thecomponent A is a specific compound selected from Tables 1 to 164, aspecific compound selected from P.1 to P.372 or a specific compoundselected from Q.001 to Q.454 and the component B is Isopyrazam. In afurther preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Sedaxane. In a further preferred embodiment the componentA is a specific compound selected from Tables 1 to 164, a specificcompound selected from P.1 to P.372 or a specific compound selected fromQ.001 to Q.454 and the component B is Boscalid. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B isFluxapyroxad. In a further preferred embodiment the component A is aspecific compound selected from Tables 1 to 164, a specific compoundselected from P.1 to P.372 or a specific compound selected from Q.001 toQ.454 and the component B is Penthiopyrad. In a further preferredembodiment the component A is a specific compound selected from Tables 1to 164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454 and the component B is Penflufen.In a further preferred embodiment the component A is a specific compoundselected from Tables 1 to 164, a specific compound selected from P.1 toP.372 or a specific compound selected from Q.001 to Q.454 and thecomponent B is Bixafen. In a further preferred embodiment the componentA is a specific compound selected from Tables 1 to 164, a specificcompound selected from P.1 to P.372 or a specific compound selected fromQ.001 to Q.454 and the component B is Fluopyram. In a further embodimentthe invention relates to a specific compound selected from Tables 1 to164, a specific compound selected from P.1 to P.372 or a specificcompound selected from Q.001 to Q.454.

The compounds of formula I, and, where appropriate, the tautomersthereof, can be present in the form of one of the isomers which arepossible or as a mixture of these, for example in the form of pureisomers, such as antipodes and/or diastereomers, or as isomer mixtures,such as structural isomer, stereo isomer, diastereoisomer and enantiomermixtures, for example racemates, diastereomer mixtures or racematemixtures, depending on the number, absolute and relative configurationof asymmetric carbon atoms which occur in the molecule and/or dependingon the configuration of non-aromatic double bonds which occur in themolecule; the invention relates to the pure isomers and also to allisomer mixtures which are possible and is to be understood in each casein this sense hereinabove and hereinbelow, even when stereochemicaldetails are not mentioned specifically in each case.

Likewise, where isomers are possible for compounds that may be selectedas component B, the invention relates to the pure isomers and also toall isomer mixtures which are possible.

The compositions according to the invention have, for practicalpurposes, a very advantageous spectrum of activities for protectinguseful plants against diseases that are caused by phytopathogenicmicroorganisms, such as fungi, bacteria or viruses.

The invention relates to a method of controlling or preventinginfestation of useful plants by phytopathogenic microorganisms, whereina composition of the invention is applied to the plants, to partsthereof or the locus thereof. The compositions according to theinvention are distinguished by excellent activity at low rates ofapplication, by being well tolerated by plants and by beingenvironmentally safe. They have very useful curative, preventive andsystemic properties and are used for protecting numerous useful plants.The compositions of the invention can be used to inhibit or destroy thediseases that occur on plants or parts of plants (fruit, blossoms,leaves, stems, tubers, roots) of different crops of useful plants, whileat the same time protecting also those parts of the plants that growlater e.g. from phytopathogenic microorganisms.

It is also possible to use compositions of the invention as dressingagents for the treatment of plant propagation material, in particular ofseeds (fruit, tubers, grains) and plant cuttings (e.g. rice), for theprotection against fungal infections as well as against phytopathogenicfungi occurring in the soil.

Furthermore the compositions of the invention may be used forcontrolling fungi in related areas, for example in the protection oftechnical materials, including wood and wood related technical products,in food storage or in hygiene management.

The compositions of the invention are, for example, effective againstthe phytopathogenic fungi of the following classes: Fungi imperfecti(e.g. Botrytis, Pyricularia, Helminthosporium, Fusarium, Septoria,Cercospora and Alternaria) and Basidiomycetes (e.g. Rhizoctonia,Hemileia, Puccinia). Additionally, they are also effective against theAscomycetes classes (e.g. Venturia and Erysiphe, Podosphaera, Monilinia,Uncinula) and of the Oomycetes classes (e.g. Phytophthora, Pythium,Plasmopara). Outstanding activity has been observed against powderymildew (Erysiphe spp.). Furthermore, the compositions of the inventionare effective against phytopathogenic bacteria and viruses (e.g. againstXanthomonas spp, Pseudomonas spp, Erwinia amylovora as well as againstthe tobacco mosaic virus). Good activity has been observed against rustdisease, like leaf rust (Puccinia spp.) and soybean rust (Phakopsorapachyrhizi).

Within the scope of the invention, useful plants to be protectedtypically comprise the following species of plants: cereal (wheat,barley, rye, oat, rice, maize, sorghum and related species); beet (sugarbeet and fodder beet); pomes, drupes and soft fruit (apples, pears,plums, peaches, almonds, cherries, strawberries, raspberries andblackberries); leguminous plants (beans, lentils, peas, soybeans); oilplants (rape, mustard, poppy, olives, sunflowers, coconut, castor oilplants, cocoa beans, groundnuts); cucumber plants (pumpkins, cucumbers,melons); fiber plants (cotton, flax, hemp, jute); citrus fruit (oranges,lemons, grapefruit, mandarins); vegetables (spinach, lettuce, asparagus,cabbages, carrots, onions, tomatoes, potatoes, paprika); lauraceae(avocado, cinnamomum, camphor) or plants such as tobacco, nuts, coffee,eggplants, sugar cane, tea, pepper, vines, hops, bananas and naturalrubber plants, as well as ornamentals and turf and grass species.

The toxin contained in the transgenic plants imparts to the plantstolerance to harmful insects. Such insects can occur in any taxonomicgroup of insects, but are especially commonly found in the beetles(Coleoptera), two-winged insects (Diptera) and butterflies(Lepidoptera).

Transgenic plants containing one or more genes that code for aninsecticidal resistance and express one or more toxins are known andsome of them are commercially available. Examples of such plants are:YieldGard® (maize variety that expresses a Cry1Ab toxin); YieldGardRootworm® (maize variety that expresses a Cry3Bb1 toxin); YieldGardPlus® (maize variety that expresses a Cry1Ab and a Cry3Bb1 toxin);Starlink® (maize variety that expresses a Cry9 C toxin); Herculex I®(maize variety that expresses a Cry1Fa2 toxin and the enzymephosphinothricine N-acetyltransferase (PAT) to achieve tolerance to theherbicide glufosinate ammonium); NuCOTN 33B® (cotton variety thatexpresses a Cry1Ac toxin); Bollgard I® (cotton variety that expresses aCry1Ac toxin); Bollgard II® (cotton variety that expresses a Cry1Ac anda Cry2Ab toxin); VipCot® (cotton variety that expresses a Vip3A and aCry1Ab toxin); NewLeaf® (potato variety that expresses a Cry3A toxin);NatureGard®, Agrisure® GT Advantage (GA21 glyphosate-tolerant trait),Agrisure® CB Advantage (Bt11 corn borer (CB) trait) and Protecta®.

Further examples of such transgenic crops are:

1. Bt11 Maize from Syngenta Seeds SAS, Chemin de l'Hobit 27, F-31 790St. Sauveur, France, registration number C/FR/96/05/10. Geneticallymodified Zea mays which have been rendered resistant to attack by theEuropean corn borer (Ostrinia nubilalis and Sesamia nonagrioides) bytransgenic expression of a truncated Cry1Ab toxin. Bt11 maize alsotransgenically expresses the enzyme PAT to achieve tolerance to theherbicide glufosinate ammonium.

2. Bt176 Maize from Syngenta Seeds SAS, Chemin de l'Hobit 27, F-31 790St. Sauveur, France, registration number C/FR/96/05/10. Geneticallymodified Zea mays which have been rendered resistant to attack by theEuropean corn borer (Ostrinia nubilalis and Sesamia nonagrioides) bytransgenic expression of a Cry1Ab toxin. Bt176 maize also transgenicallyexpresses the enzyme PAT to achieve tolerance to the herbicideglufosinate ammonium.

3. MIR604Maize from Syngenta Seeds SAS, Chemin de l'Hobit 27, F-31 790St. Sauveur, France, registration number C/FR/96/05/10. Maize which hasbeen rendered insect-resistant by transgenic expression of a modifiedCry3A toxin. This toxin is Cry3A055 modified by insertion of acathepsin-G-protease recognition sequence. The preparation of suchtransgenic maize plants is described in WO 03/018810.

4. MON 863 Maize from Monsanto Europe S.A. 270-272 Avenue de Tervuren,B-1150 Brussels, Belgium, registration number C/DE/02/9. MON 863expresses a Cry3Bb1 toxin and has resistance to certain Coleopterainsects.

5. IPC 531 Cotton from Monsanto Europe S.A. 270-272 Avenue de Tervuren,B-1150 Brussels, Belgium, registration number C/ES/96/02.

6. 1507 Maize from Pioneer Overseas Corporation, Avenue Tedesco, 7B-1160 Brussels, Belgium, registration number C/N L/00/10. Geneticallymodified maize for the expression of the protein Cry1 F for achievingresistance to certain Lepidoptera insects and of the PAT protein forachieving tolerance to the herbicide glufosinate ammonium.

7. NK603×MON 810 Maize from Monsanto Europe S.A. 270-272 Avenue deTervuren, B-1150 Brussels, Belgium, registration number C/GB/02/M3/03.Consists of conventionally bred hybrid maize varieties by crossing thegenetically modified varieties NK603 and MON 810. NK603×MON 810 Maizetransgenically expresses the protein CP4 EPSPS, obtained fromAgrobacterium sp. strain CP4, which imparts tolerance to the herbicideRoundup® (contains glyphosate), and also a Cry1Ab toxin obtained fromBacillus thuringiensis subsp. kurstaki which brings about tolerance tocertain Lepidoptera, include the European corn borer.

The term “locus” of a useful plant as used herein is intended to embracethe place on which the useful plants are growing, where the plantpropagation materials of the useful plants are sown or where the plantpropagation materials of the useful plants will be placed into the soil.An example for such a locus is a field, on which crop plants aregrowing.

The term “plant propagation material” is understood to denote generativeparts of the plant, such as seeds, which can be used for themultiplication of the latter, and vegetative material, such as cuttingsor tubers, for example potatoes. There may be mentioned for exampleseeds (in the strict sense), roots, fruits, tubers, bulbs, rhizomes andparts of plants. Germinated plants and young plants which are to betransplanted after germination or after emergence from the soil, mayalso be mentioned. These young plants may be protected beforetransplantation by a total or partial treatment by immersion. Preferably“plant propagation material” is understood to denote seeds.

Components A and B can be used in unmodified form or, preferably,together with carriers and adjuvants conventionally employed in the artof formulation.

To this components A and B and inert carriers are convenientlyformulated in known manner to emulsifiable concentrates, coatablepastes, directly sprayable or dilutable solutions, dilute emulsions,wettable powders, soluble powders, dusts, granulates, and alsoencapsulations e.g. in polymeric substances. As with the type of thecompositions, the methods of application, such as spraying, atomizing,dusting, scattering, coating or pouring, are chosen in accordance withthe intended objectives and the prevailing circumstances. Thecompositions may also contain further adjuvants such as stabilizers,antifoams, viscosity regulators, binders or tackifiers as well asfertilizers, micronutrient donors or other formulations for obtainingspecial effects.

Suitable carriers and adjuvants can be solid or liquid and aresubstances useful in formulation technology, e.g. natural or regeneratedmineral substances, solvents, dispersants, wetting agents, tackifiers,thickeners, binders or fertilizers. Such carriers are for exampledescribed in WO 97/33890.

The compositions of the invention can be applied to the locus of theplant or plant to be treated, simultaneously or in succession withfurther compounds. These further compounds can be e.g. fertilizers ormicronutrient donors or other preparations which influence the growth ofplants. They can also be herbicides as well as insecticides, fungicides,bactericides, nematicides, molluscicides or mixtures of several of thesepreparations, if desired together with further carriers, surfactants orapplication promoting adjuvants customarily employed in the art offormulation. Suitable further compounds are described in WO2008/101682.

A preferred method of the invention is foliar application. The frequencyof application and the rate of application will depend on the risk ofinfestation by the corresponding pathogen. However, the compositions ofthe invention can also penetrate the plant through the roots via thesoil (systemic action) by drenching the locus of the plant with a liquidformulation, or by applying the compounds in solid form to the soil,e.g. in granular form (soil application). In crops of water rice suchgranulates can be applied to the flooded rice field. The compositions ofthe invention may also be applied to seeds (coating) by impregnating theseeds or tubers either with a liquid formulation of the fungicide orcoating them with a solid formulation.

A formulation, i.e. a composition of the invention and, if desired,comprising a solid or liquid adjuvant, is prepared in a known manner,typically by intimately mixing and/or grinding the compound withextenders, for example solvents, solid carriers and, optionally,surface-active compounds (surfactants).

The agrochemical formulations will usually contain from 0.1 to 99% byweight, preferably from 0.1 to 95% by weight, of the active ingredients,99.9 to 1% by weight, preferably 99.8 to 5% by weight, of a solid orliquid adjuvant, and from 0 to 25% by weight, preferably from 0.1 to 25%by weight, of a surfactant.

Whereas it is preferred to formulate commercial products asconcentrates, the end user will normally use dilute formulations.

Advantageous rates of application are normally from 1 g to 2 kg ofactive ingredient (a.i.) per hectare (ha), preferably from 10 g to 1 kga.i./ha, most preferably from 20 g to 600 g a.i./ha. When used as seeddrenching agent, convenient rates of application are from 10 mg to 1 gof active substance per kg of seeds. The rate of application for thedesired action can be determined by experiments. It depends for exampleon the type of action, the developmental stage of the useful plant, andon the application (location, timing, application method) and can, owingto these parameters, vary within wide limits.

Said methods are particularly effective against the phytopathogenicorganisms of the kingdom Fungi, phylum Basidiomycot, classUredinomycetes, subclass Urediniomycetidae and the order Uredinales(commonly referred to as rusts). Species of rusts having a particularlylarge impact on agriculture include those of the family Phakopsoraceae,particularly those of the genus Phakopsora, for example Phakopsorapachyrhizi, which is also referred to as Asian soybean rust, and thoseof the family Pucciniaceae, particularly those of the genus Pucciniasuch as Puccinia graminis, also known as stem rust or black rust, whichis a problem disease in cereal crops and Puccinia recondita, also knownas brown rust.

The compositions of the invention are effective against variousmicrobial species able to cause a microbial infection in an animal.Examples of such microbial species are those causing Aspergillosis suchas Aspergillus fumigatus, A. flavus, A. terrus, A. nidulans and A.niger, those causing Blastomycosis such as Blastomyces dermatitidis;those causing Candidiasis such as Candida albicans, C. glabrata, C.tropicalis, C. parapsilosis, C. krusei and C. lusitaniae; those causingCoccidioidomycosis such as Coccidioides immitis; those causingCryptococcosis such as Cryptococcus neoformans; those causingHistoplasmosis such as Histoplasma capsulatum and those causingZygomycosis such as Absidia corymbifera, Rhizomucor pusillus andRhizopus arrhizus. Further examples are Fusarium Spp such as Fusariumoxysporum and Fusarium solani and Scedosporium Spp such as Scedosporiumapiospermum and Scedosporium prolificans. Still further examples areMicrosporum Spp, Trichophyton Spp, Epidermophyton Spp, Mucor Spp,Sporothorix Spp, Phialophora Spp, Cladosporium Spp, Petriellidium spp,Paracoccidioides Spp and Histoplasma Spp.

The following table provides a selection of compounds of the invention

Cpd No. Structure P.01

P.02

P.03

P.04

P.05

P.06

P.07

P.08

P.09

P.10

P.11

P.12

P.13

P.14

P.15

P.16

P.17

P.18

P.19

P.20

P.21

P.22

P.23

P.24

P.25

P.26

P.27

P.28

P.29

P.30

P.31

P.32

P.33

P.34

P.35

P.36

P.37

P.38

P.39

P.40

P.41

P.42

P.43

P.44

P.45

P.46

P.47

P.48

P.49

P.50

P.51

P.52

P.53

P.54

P.55

P.56

P.57

P.58

P.59

P.60

P.61

P.62

P.63

P.64

P.65

P.66

P.67

P.68

P.69

P.70

P.71

P.72

P.73

P.74

P.75

P.76

P.77

P.78

P.79

P.80

P.81

P.82

P.83

P.84

P.85

P.86

P.87

P.88

P.89

P.90

P.91

P.92

P.93

P.94

P.95

P.96

P.97

P.98

P.99

P.100

P.101

P.101a

P.102

P.103

P.104

P.105

P.106

P.107

P.108

P.109

P.110

P.111

P.112

P.113

P.114

P.115

P.116

P.117

P.118

P.119

P.120

P.121

P.122

P.123

P.124

P.125

P.126

P.127

P.128

P.129

P.130

P.131

P.132

P.133

P.134

P.135

P.136

P.137

P.138

P.139

P.140

P.141

P.142

P.143

P.145

P.146

P.147

P.148

P.149

P.150

P.151

P.152

P.153

P.154

P.155

P.156

P.157

P.158

P.159

P.160

P.161

P.162

P.163

P.164

P.165

P.166

P.167

P.168

P.169

P.170

P.171

P.172

P.173

P.174

P.175

P.176

P.177

P.178

P.179

P.180

P.181

P.182

P.183

P.184

P.185

P.186

P.187

P.188

P.189

P.190

P.191

P.192

P.193

P.194

P.195

P.196

P.197

P.198

P.199

P.200

P.201

P.202

P.203

P.204

P.205

P.206

P.207

P.208

P.209

P.210

P.211

P.212

P.213

P.214

P.215

P.216

P.217

P.218

P.219

P.220

P.221

P.222

P.223

P.224

P.225

P.226

P.227

P.228

P.229

P.230

P.231

P.232

P.233

P.234

P.235

P.236

P.237

P.238

P.239

P.240

P.241

P.242

P.243

P.244

P.245

P.246

P.247

P.248

P.249

P.250

P.251

P.252

P.253

P.254

P.255

P.256

P.257

P.258

P.259

P.260

P.261

P.262

P.263

P.264

P.265

P.266

P.267

P.268

P.269

P.270

P.271

P.272

P.273

P.274

P.275

P.276

P.277

P.278

P.279

P.280

P.281

P.282

P.283

P.284

P.285

P.286

P.287

P.288

P.289

P.290

P.291

P.292

P.293

P.294

P.295

P.296

P.297

P.298

P.299

P.300

P.301

P.302

P.303

P.304

P.305

P.306

P.307

P.308

P.309

P.310

P.311

P.312

P.313

P.314

P.315

P.316

P.317

P.318

P.319

P.320

P.321

P.322

P.323

P.324

P.325

P.326

P.327

P.328

P.329

P.330

P.331

P.332

P.333

P.334

P.335

P.336

P.337

P.338

P.339

P.340

P.341

P.342

P.343

P.344

P.345

P.346

P.347

P.348

P.349

P.350

P.351

P.352

P.353

P.354

P.355

P.356

P.357

P.358

P.359

P.360

P.361

P.362

P.363

P.364

P.365

P.366

P.367

P.368

P.369

P.370

P.371

P.372

Table A discloses 1201 sets of meanings of the variables R₁, R₂, R₅ andR₆ in a compound of formula I.

TABLE A Meanings for R₁, R₂, R₅ and R₆: Line R₁ R₂ R₆ R₅ A.1.1 CH₃CH₂CH₃ H

A.1.2 CH₃ CH₂CH₃ H

A.1.3 CH₃ CH₂CH₃ H

A.1.4 CH₃ CH₂CH₃ H

A.1.5 CH₃ CH₂CH₃ H

A.1.6 CH₃ CH₂CH₃ H

A.1.7 CH₃ CH₂CH₃ H

A.1.8 CH₃ CH₂CH₃ H

A.1.9 CH₃ CH₂CH₃ H

A.1.10 CH₃ CH₂CH₃ H

A.1.11 CH₃ CH₂CH₃ H

A.1.12 CH₃ CH₂CH₃ H

A.1.13 CH₃ CH₂CH₃ H

A.1.14 CH₃ CH₂CH₃ H

A.1.15 CH₃ CH₂CH₃ H

A.1.16 CH₃ CH₂CH₃ H

A.1.17 CH₃ CH₂CH₃ H

A.1.18 CH₃ CH₂CH₃ H

A.1.19 CH₃ CH₂CH₃ H

A.1.20 CH₃ CH₂CH₃ H

A.1.21 CH₃ CH₂CH₃ H

A.1.22 CH₃ CH₂CH₃ H

A.1.23 CH₃ CH₂CH₃ H

A.1.24 CH₃ CH₂CH₃ H

A.1.25 CH₃ CH₂CH₃ H

A.1.26 CH₃ CH₂CH₃ H

A.1.27 CH₃ CH₂CH₃ H

A.1.28 CH₃ CH₂CH₃ H

A.1.29 CH₃ CH₂CH₃ H

A.1.30 CH₃ CH₂CH₃ H

A.1.31 CH₃ CH₂CH₃ H

A.1.32 CH₃ CH₂CH₃ H

A.1.33 CH₃ CH₂CH₃ H

A.1.34 CH₃ CH₂CH₃ H

A.1.35 CH₃ CH₂CH₃ H

A.1.36 CH₃ CH₂CH₃ H

A.1.37 CH₃ CH₂CH₃ H

A.1.38 CH₃ CH₂CH₃ H

A.1.39 CH₃ CH₂CH₃ H

A.1.40 CH₃ CH₂CH₃ H

A.1.41 CH₃ CH₂CH₃ H

A.1.42 CH₃ CH₂CH₃ H

A.1.43 CH₃ CH₂CH₃ H

A.1.44 CH₃ CH₂CH₃ H

A.1.45 CH₃ CH₂CH₃ H

A.1.46 CH₃ CH₂CH₃ H

A.1.47 CH₃ CH₂CH₃ H

A.1.48 CH₃ CH₂CH₃ H

A.1.49 CH₃ CH₂CH₃ H

A.1.50 CH₃ CH₂CH₃ H

A.1.51 CH₃ CH₂CH₃ H

A.1.52 CH₃ CH₂CH₃ H

A.1.53 CH₃ CH₂CH₃ H

A.1.54 CH₃ CH₂CH₃ H

A.1.55 CH₃ CH₂CH₃ H

A.1.56 CH₃ CH₂CH₃ H

A.1.57 CH₃ CH₂CH₃ H

A.1.58 CH₃ CH₂CH₃ H

A.1.59 CH₃ CH₂CH₃ H

A.1.60 CH₃ CH₂CH₃ H

A.1.61 CH₃ CH₂CH₃ H

A.1.62 CH₃ CH₂CH₃ H

A.1.63 CH₃ CH₂CH₃ H

A.1.64 CH₃ CH₂CH₃ H

A.1.65 CH₃ CH₂CH₃ H

A.1.66 CH₃ CH₂CH₃ H

A.1.67 CH₃ CH₂CH₃ H

A.1.68 CH₃ CH₂CH₃ H

A.1.69 CH₃ CH₂CH₃ H

A.1.70 CH₃ CH₂CH₃ H

A.1.71 CH₃ CH₂CH₃ H

A.1.72 CH₃ CH₂CH₃ H

A.1.73 CH₃ CH₂CH₃ H

A.1.74 CH₃ CH₂CH₃ H

A.1.75 CH₃ CH₂CH₃ H

A.1.76 CH₃ CH₂CH₃ H

A.1.77 CH₃ CH₂CH₃ H

A.1.78 CH₃ CH₂CH₃ H

A.1.79 CH₃ CH₂CH₃ H

A.1.80 CH₃ CH₂CH₃ H

A.1.81 CH₃ CH₂CH₃ H

A.1.82 CH₃ CH₂CH₃ H

A.1.83 CH₃ CH₂CH₃ H

A.1.84 CH₃ CH₂CH₃ H

A.1.85 CH₃ CH₂CH₃ H

A.1.86 CH₃ CH₂CH₃ H

A.1.87 CH₃ CH₂CH₃ H

A.1.88 CH₃ CH₂CH₃ H

A.1.89 CH₃ CH₂CH₃ H

A.1.90 CH₃ CH₂CH₃ H

A.1.91 CH₃ CH₂CH₃ H

A.1.92 CH₃ CH₂CH₃ H

A.1.93 CH₃ CH₂CH₃ H

A.1.94 CH₃ CH₂CH₃ H

A.1.95 CH₃ CH₂CH₃ H

A.1.96 CH₃ CH₂CH₃ H

A.1.97 CH₃ CH₂CH₃ H

A.1.98 CH₃ CH₂CH₃ H

A.1.99 CH₃ CH₂CH₃ H

A.1.100 CH₃ CH₂CH₃ H

A.1.101 CH₃ CH₂CH₃ H

A.1.102 CH₃ CH₂CH₃ H

A.1.103 CH₃ CH₂CH₃ H

A.1.104 CH₃ CH₂CH₃ H

A.1.105 CH₃ CH₂CH₃ H

A.1.106 CH₃ CH₂CH₃ H

A.1.107 CH₃ CH₂CH₃ H

A.1.108 CH₃ CH₂CH₃ H

A.1.109 CH₃ CH₂CH₃ H

A.1.110 CH₃ CH₂CH₃ H

A.1.111 CH₃ CH₂CH₃ H

A.1.112 CH₃ CH₂CH₃ H

A.1.113 CH₃ CH₂CH₃ H

A.1.114 CH₃ CH₂CH₃ H

A.1.115 CH₃ CH₂CH₃ H

A.1.116 CH₃ CH₂CH₃ H

A.1.117 CH₃ CH₂CH₃ H

A.1.118 CH₃ CH₂CH₃ H

A.1.119 CH₃ CH₂CH₃ H

A.1.120 CH₃ CH₂CH₃ H

A.1.121 CH₃ CH₂CH₃ H

A.1.122 CH₃ CH₂CH₃ H

A.1.123 CH₃ CH₂CH₃ H

A.1.124 CH₃ CH₂CH₃ H

A.1.125 CH₃ CH₂CH₃ H

A.1.126 CH₃ CH₂CH₃ H

A.1.127 CH₃ CH₂CH₃ H

A.1.128 CH₃ CH₂CH₃ H

A.1.129 CH₃ CH₂CH₃ H

A.1.130 CH₃ CH₂CH₃ H

A.1.131 CH₃ CH₂CH₃ H

A.1.132 CH₃ CH₂CH₃ H

A.1.133 CH₃ CH₂CH₃ H

A.1.134 CH₃ CH₂CH₃ H

A.1.135 CH₃ CH₂CH₃ H

A.1.136 CH₃ CH₂CH₃ H

A.1.137 CH₃ CH₂CH₃ H

A.1.138 CH₃ CH₂CH₃ H

A.1.139 CH₃ CH₂CH₃ H

A.1.140 CH₃ CH₂CH₃ H

A.1.141 CH₃ CH₂CH₃ H

A.1.142 CH₃ CH₂CH₃ H

A.1.143 CH₃ CH₂CH₃ H

A.1.144 CH₃ CH₂CH₃ H

A.1.145 CH₃ CH₂CH₃ H

A.1.146 CH₃ CH₂CH₃ H

A.1.147 CH₃ CH₂CH₃ H

A.1.148 CH₃ CH₂CH₃ H

A.1.149 CH₃ CH₂CH₃ H

A.1.150 CH₃ CH₂CH₃ H

A.1.151 CH₃ CH₂CH₃ H

A.1.152 CH₃ CH₂CH₃ H

A.1.153 CH₃ CH₂CH₃ H

A.1.154 CH₃ CH₂CH₃ H

A.1.155 CH₃ CH₂CH₃ H

A.1.156 CH₃ CH₂CH₃ H

A.1.157 CH₃ CH₂CH₃ H

A.1.158 CH₃ CH₂CH₃ H

A.1.159 CH₃ CH₂CH₃ H

A.1.160 CH₃ CH₂CH₃ H

A.1.161 CH₃ CH₂CH₃ H

A.1.162 CH₃ CH₂CH₃ H

A.1.163 CH₃ CH₂CH₃ H

A.1.164 CH₃ CH₂CH₃ H

A.1.165 CH₃ CH₂CH₃ H

A.1.166 CH₃ CH₂CH₃ H

A.1.167 CH₃ CH₂CH₃ H

A.1.168 CH₃ CH₂CH₃ H

A.1.169 CH₃ CH₂CH₃ H

A.1.170 CH₃ CH₂CH₃ H

A.1.171 CH₃ CH₂CH₃ H

A.1.172 CH₃ CH₂CH₃ H

A.1.173 CH₃ CH₂CH₃ H

A.1.174 CH₃ CH₂CH₃ H

A.1.175 CH₃ CH₂CH₃ H

A.1.176 CH₃ CH₂CH₃ H

A.1.177 CH₃ CH₂CH₃ H

A.1.178 CH₃ CH₂CH₃ H

A.1.179 CH₃ CH₂CH₃ H

A.1.180 CH₃ CH₂CH₃ H

A.1.181 CH₃ CH₂CH₃ H

A.1.182 CH₃ CH₂CH₃ H

A.1.183 CH₃ CH₂CH₃ H

A.1.184 CH₃ CH₂CH₃ H

A.1.185 CH₃ CH₂CH₃ H

A.1.186 CH₃ CH₂CH₃ H

A.1.187 CH₃ CH₂CH₃ H

A.1.188 CH₃ CH₂CH₃ H

A.1.189 CH₃ CH₂CH₃ H

A.1.190 CH₃ CH₂CH₃ H

A.1.191 CH₃ CH₂CH₃ H

A.1.192 CH₃ CH₂CH₃ H

A.1.193 CH₃ CH₂CH₃ H

A.1.194 CH₃ CH₂CH₃ H

A.1.195 CH₃ CH₂CH₃ H

A.1.196 CH₃ CH₂CH₃ H

A.1.197 CH₃ CH₂CH₃ H

A.1.198 CH₃ CH₂CH₃ H

A.1.199 CH₃ CH₂CH₃ H

A.1.200 CH₃ CH₂CH₃ H

A.1.201 CH₃ CH₂CH₃ H

A.1.202 CH₃ CH₂CH₃ H

A.1.203 CH₃ CH₂CH₃ H

A.1.204 CH₃ CH₂CH₃ H

A.1.205 CH₃ CH₂CH₃ H

A.1.206 CH₃ CH₂CH₃ H

A.1.207 CH₃ CH₂CH₃ H

A.1.208 CH₃ CH₂CH₃ H

A.1.209 CH₃ CH₂CH₃ H

A.1.210 CH₃ CH₂CH₃ H

A.1.211 CH₃ CH₂CH₃ H

A.1.212 CH₃ CH₂CH₃ H

A.1.213 CH₃ CH₂CH₃ H

A.1.214 CH₃ CH₂CH₃ H

A.1.215 CH₃ CH₂CH₃ H

A.1.216 CH₃ CH₂CH₃ H

A.1.217 CH₃ CH₂CH₃ H

A.1.218 CH₃ CH₂CH₃ H

A.1.219 CH₃ CH₂CH₃ H

A.1.220 CH₃ CH₂CH₃ H

A.1.221 CH₃ CH₂CH₃ H

A.1.222 CH₃ CH₂CH₃ H

A.1.223 CH₃ CH₂CH₃ H

A.1.224 CH₃ CH₂CH₃ H

A.1.225 CH₃ CH₂CH₃ H

A.1.226 CH₃ CH₂CH₃ H

A.1.227 CH₃ CH₂CH₃ H

A.1.228 CH₃ CH₂CH₃ H

A.1.229 CH₃ CH₂CH₃ H

A.1.230 CH₃ CH₂CH₃ H

A.1.231 CH₃ CH₂CH₃ H

A.1.232 CH₃ CH₂CH₃ H H— A.1.233 CH₃ CH₂CH₃ H

A.1.234 CH₃ CH₂CH₃ H

A.1.235 CH₃ CH₂CH₃ H

A.1.236 CH₃ CH₂CH₃ H

A.1.237 CH₃ CH₂CH₃ H

A.1.238 CH₃ CH₂CH₃ H

A.1.239 CH₃ CH₂CH₃ H

A.1.240 CH₃ CH₂CH₃ H

A.1.241 CH₃ CH₂CH₃ H

A.1.242 CH₃ CH₂CH₃ H

A.1.243 CH₃ CH₂CH₃ H

A.1.244 CH₃ CH₂CH₃ H

A.1.245 CH₃ CH₂CH₃ H H₃C— A.1.246 CH₃ CH₂CH₃ H

A.1.247 CH₃ CH₂CH₃ H

A.1.248 CH₃ CH₂CH₃ H

A.1.249 CH₃ CH₂CH₃ H

A.1.250 CH₃ CH₂CH₃ H

A.1.251 CH₃ CH₂CH₃ H

A.1.252 CH₃ CH₂CH₃ H

A.1.253 CH₃ CH₂CH₃ H

A.1.254 CH₃ CH₂CH₃ H

A.1.255 CH₃ CH₂CH₃ H

A.1.256 CH₃ CH₂CH₃ H

A.1.257 CH₃ CH₂CH₃ H

A.1.258 CH₃ CH₂CH₃ H

A.1.259 CH₃ CH₂CH₃ H

A.1.260 CH₃ CH₂CH₃ H

A.1.261 CH₃ CH₂CH₃ H

A.1.262 CH₃ CH₂CH₃ H

A.1.263 CH₃ CH₂CH₃ H

A.1.264 CH₃ CH₂CH₃ H

A.1.265 CH₃ CH₂CH₃ H

A.1.266 CH₃ CH₂CH₃ H

A.1.267 CH₃ CH₂CH₃ H

A.1.268 CH₃ CH₂CH₃ H

A.1.269 CH₃ CH₂CH₃ H

A.1.270 CH₃ CH₂CH₃ H

A.1.271 CH₃ CH₂CH₃ H

A.1.272 CH₃ CH₂CH₃ H

A.1.273 CH₃ CH₂CH₃ H

A.1.274 CH₃ CH₂CH₃ H

A.1.275 CH₃ CH₂CH₃ H

A.1.276 CH₃ CH₂CH₃ H

A.1.277 CH₃ CH₂CH₃ H

A.1.278 CH₃ CH₂CH₃ H

A.1.279 CH₃ CH₂CH₃ H

A.1.280 CH₃ CH₂CH₃ H

A.1.281 CH₃ CH₂CH₃ H

A.1.282 CH₃ CH₂CH₃ H

A.1.283 CH₃ CH₂CH₃ H

A.1.284 CH₃ CH₂CH₃ H

A.1.285 CH₃ CH₂CH₃ H

A.1.286 CH₃ CH₂CH₃ H

A.1.287 CH₃ CH₂CH₃ H

A.1.288 CH₃ CH₂CH₃ H

A.1.289 CH₃ CH₂CH₃ H

A.1.290 CH₃ CH₂CH₃ H

A.1.291 CH₃ CH₂CH₃ H

A.1.292 CH₃ CH₂CH₃ H

A.1.293 CH₃ CH₂CH₃ H

A.1.294 CH₃ CH₂CH₃ H

A.1.295 CH₃ CH₂CH₃ H

A.1.296 CH₃ CH₂CH₃ H

A.1.297 CH₃ CH₂CH₃ H

A.1.298 CH₃ CH₂CH₃ H

A.1.299 CH₃ CH₂CH₃ H

A.1.300 CH₃ CH₂CH₃ H

A.1.301 CH₃ CH₂CH₃ H

A.1.302 CH₃ CH₂CH₃ H

A.1.303 CH₃ CH₂CH₃ H

A.1.304 CH₃ CH₂CH₃ H

A.1.305 CH₃ CH₂CH₃ H

A.1.306 CH₃ CH₂CH₃ H

A.1.307 CH₃ CH₂CH₃ H

A.1.308 CH₃ CH₂CH₃ H

A.1.309 CH₃ CH₂CH₃ H

A.1.310 CH₃ CH₂CH₃ H

A.1.311 CH₃ CH₂CH₃ H

A.1.312 CH₃ CH₂CH₃ H

A.1.313 CH₃ CH₂CH₃ H

A.1.314 CH₃ CH₂CH₃ H

A.1.315 CH₃ CH₂CH₃ H

A.1.316 CH₃ CH₂CH₃ H

A.1.317 CH₃ CH₂CH₃ H

A.1.318 CH₃ CH₂CH₃ H

A.1.319 CH₃ CH₂CH₃ H

A.1.320 CH₃ CH₂CH₃ H

A.1.321 CH₃ CH₂CH₃ H

A.1.322 CH₃ CH₂CH₃ H

A.1.323 CH₃ CH₂CH₃ H

A.1.324 CH₃ CH₂CH₃ H

A.1.325 CH₃ CH₂CH₃ H

A.1.326 CH₃ CH₂CH₃ H

A.1.327 CH₃ CH₂CH₃ H

A.1.328 CH₃ CH₂CH₃ H

A.1.329 CH₃ CH₂CH₃ H

A.1.330 CH₃ CH₂CH₃ H

A.1.331 CH₃ CH₂CH₃ H

A.1.332 CH₃ CH₂CH₃ H

A.1.333 CH₃ CH₂CH₃ H

A.1.334 CH₃ CH₂CH₃ H

A.1.335 CH₃ CH₂CH₃ H

A.1.336 CH₃ CH₂CH₃ H

A.1.337 CH₃ CH₂CH₃ H

A.1.338 CH₃ CH₂CH₃ H

A.1.339 CH₃ CH₂CH₃ H

A.1.340 CH₃ CH₂CH₃ H

A.1.341 CH₃ CH₂CH₃ H

A.1.342 CH₃ CH₂CH₃ H

A.1.343 CH₃ CH₂CH₃ H

A.1.344 CH₃ CH₂CH₃ H

A.1.345 CH₃ CH₂CH₃ H

A.1.346 CH₃ CH₂CH₃ H

A.1.347 CH₃ CH₂CH₃ H

A.1.348 CH₃ CH₂CH₃ H

A.1.349 CH₃ CH₂CH₃ H

A.1.350 CH₃ CH₂CH₃ H

A.1.351 CH₃ CH₂CH₃ H

A.1.352 CH₃ CH₂CH₃ H

A.1.353 CH₃ CH₂CH₃ H

A.1.354 CH₃ CH₂CH₃ H

A.1.355 CH₃ CH₂CH₃ H

A.1.356 CH₃ CH₂CH₃ H

A.1.357 CH₃ CH₂CH₃ H

A.1.358 CH₃ CH₂CH₃ H

A.1.359 CH₃ CH₂CH₃ H

A.1.360 CH₃ CH₂CH₃ H

A.1.361 CH₃ CH₂CH₃ H

A.1.362 CH₃ CH₂CH₃ H

A.1.363 CH₃ CH₂CH₃ H

A.1.364 CH₃ CH₂CH₃ H

A.1.365 CH₃ CH₂CH₃ H

A.1.366 CH₃ CH₂CH₃ H

A.1.367 CH₃ CH₂CH₃ H

A.1.368 CH₃ CH₂CH₃ H

A.1.369 CH₃ CH₂CH₃ H

A.1.370 CH₃ CH₂CH₃ H

A.1.371 CH₃ CH₂CH₃ H

A.1.372 CH₃ CH₂CH₃ H

A.1.373 CH₃ CH₂CH₃ H

A.1.374 CH₃ CH₂CH₃ H

A.1.375 CH₃ CH₂CH₃ H

A.1.376 CH₃ CH₂CH₃ H

A.1.377 CH₃ CH₂CH₃ H

A.1.378 CH₃ CH₂CH₃ H

A.1.379 CH₃ CH₂CH₃ H

A.1.380 CH₃ CH₂CH₃ H

A.1.381 CH₃ CH₂CH₃ H

A.1.382 CH₃ CH₂CH₃ H

A.1.383 CH₃ CH₂CH₃ H

A.1.384 CH₃ CH₂CH₃ H

A.1.385 CH₃ CH₂CH₃ H

A.1.386 CH₃ CH₂CH₃ H

A.1.387 CH₃ CH₂CH₃ H

A.1.388 CH₃ CH₂CH₃ H

A.1.389 CH₃ CH₂CH₃ H

A.1.390 CH₃ CH₂CH₃ H

A.1.391 CH₃ CH₂CH₃ H

A.1.392 CH₃ CH₂CH₃ H

A.1.393 CH₃ CH₂CH₃ H

A.1.394 CH₃ CH₂CH₃ H

A.1.395 CH₃ CH₂CH₃ H

A.1.396 CH₃ CH₂CH₃ H

A.1.397 CH₃ CH₂CH₃ H

A.1.398 CH₃ CH₂CH₃ H

A.1.399 CH₃ CH₂CH₃ H

A.1.400 CH₃ CH₂CH₃ H

A.1.401 CH₃ CH₂CH₃ H

A.1.402 CH₃ CH₂CH₃ H

A.1.403 CH₃ CH₂CH₃ H

A.1.404 CH₃ CH₂CH₃ H

A.1.405 CH₃ CH₂CH₃ H

A.1.406 CH₃ CH₂CH₃ H

A.1.407 CH₃ CH₂CH₃ H

A.1.408 CH₃ CH₂CH₃ H

A.1.409 CH₃ CH₂CH₃ H

A.1.410 CH₃ CH₂CH₃ H

A.1.411 CH₃ CH₂CH₃ H

A.1.412 CH₃ CH₂CH₃ H

A.1.413 CH₃ CH₂CH₃ H

A.1.414 CH₃ CH₂CH₃ H

A.1.415 CH₃ CH₂CH₃ H

A.1.416 CH₃ CH₂CH₃ H

A.1.417 CH₃ CH₂CH₃ H

A.1.418 CH₃ CH₂CH₃ H

A.1.419 CH₃ CH₂CH₃ H

A.1.420 CH₃ CH₂CH₃ H

A.1.421 CH₃ CH₂CH₃ H

A.1.422 CH₃ CH₂CH₃ H

A.1.423 CH₃ CH₂CH₃ H

A.1.424 CH₃ CH₂CH₃ H

A.1.425 CH₃ CH₂CH₃ H

A.1.426 CH₃ CH₂CH₃ H

A.1.427 CH₃ CH₂CH₃ H

A.1.428 CH₃ CH₂CH₃ H

A.1.429 CH₃ CH₂CH₃ H

A.1.430 CH₃ CH₂CH₃ H

A.1.431 CH₃ CH₂CH₃ H

A.1.432 CH₃ CH₂CH₃ H

A.1.433 CH₃ CH₂CH₃ H

A.1.434 CH₃ CH₂CH₃ H

A.1.435 CH₃ CH₂CH₃ H

A.1.436 CH₃ CH₂CH₃ H

          Line

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A.1.983

A.1.984

A.1.985

A.1.986

A.1.987

A.1.988

A.1.989

A.1.990

A.1.991

A.1.992

A.1.993

A.1.994

A.1.995

A.1.996

A.1.997

A.1.998

A.1.999

A.1.1000

A.1.1001

A.1.1002

A.1.1003

A.1.1004

A.1.1005

A.1.1006

A.1.1007

A.1.1008

A.1.1009

A.1.1010

A.1.1011

A.1.1012

A.1.1013

A.1.1014

A.1.1015

A.1.1016

A.1.1017

A.1.1018

A.1.1019

A.1.1020

A.1.1021

A.1.1022

A.1.1023

A.1.1024

A.1.1025

A.1.1026

H—# A.1.1027

H—# A.1.1028

H—# A.1.1029

H—# A.1.1030

H—# A.1.1031

H—# A.1.1032

H—# A.1.1033

H—# A.1.1034

A.1.1035

A.1.1036

A.1.1037

A.1.1038

A.1.1039

A.1.1040

A.1.1041

A.1.1042

A.1.1043

A.1.1044

A.1.1045

A.1.1046

A.1.1047

A.1.1048

A.1.1049

A.1.1050

A.1.1051

A.1.1052

A.1.1053

A.1.1054

A.1.1055

A.1.1056

A.1.1057

A.1.1058

A.1.1059

A.1.1060

A.1.1061

A.1.1062

A.1.1063

A.1.1064

A.1.1065

A.1.1066

A.1.1067

A.1.1068

A.1.1069

A.1.1070

A.1.1071

A.1.1072

A.1.1073

A.1.1074

A.1.1075

A.1.1076

A.1.1077

A.1.1078

A.1.1079

A.1.1080

A.1.1081

A.1.1082

A.1.1083

A.1.1084

A.1.1085

A.1.1086

A.1.1087

A.1.1088

A.1.1089

A.1.1090

A.1.1091

A.1.1092

A.1.1093

A.1.1094

A.1.1095

A.1.1096

A.1.1097

A.1.1098

A.1.1099

A.1.1100

A.1.1101

A.1.1102

A.1.1103

A.1.1104

A.1.1105

A.1.1106

A.1.1107

A.1.1108

A.1.1109

A.1.1110

A.1.1111

A.1.1112

A.1.1113

A.1.1114

A.1.1115

A.1.1116

A.1.1117

A.1.1118

A.1.1119

A.1.1120

A.1.1121

A.1.1122

A.1.1123

A.1.1124

A.1.1125

A.1.1126

A.1.1127

A.1.1128

A.1.1129

A.1.1130

A.1.1131

A.1.1132

A.1.1133

A.1.1134

A.1.1135

A.1.1136

A.1.1137

A.1.1138

A.1.1139

A.1.1140

A.1.1141

A.1.1142

A.1.1143

A.1.1144

A.1.1145

A.1.1146

A.1.1147

A.1.1148

A.1.1149

A.1.1150

A.1.1151

A.1.1152

A.1.1153

A.1.1154

A.1.1155

A.1.1156

A.1.1157

A.1.1158

A.1.1159

A.1.1160

A.1.1161

A.1.1162

A.1.1163

A.1.1164

A.1.1165

A.1.1166

A.1.1167

A.1.1168

A.1.1169

A.1.1170

A.1.1171

A.1.1172

A.1.1173

A.1.1174

A.1.1175

A.1.1176

A.1.1177

A.1.1178

A.1.1179

A.1.1180

A.1.1181

A.1.1182

A.1.1183

A.1.1184

A.1.1185

A.1.1186

A.1.1187

A.1.1188

A.1.1189

A.1.1190

A.1.1191

A.1.1192

A.1.1193

A.1.1194

A.1.1195

A.1.1196

A.1.1197

A.1.1198

A.1.1199

A.1.1200

A.1.1201

The following tables T1 to T151 disclose preferred compounds of formulaI for inclusion as component A in compositions of the invention.

TABLE 1 This table discloses the 1201 compounds T1.1.1 to T1.1.1201 ofthe formula (T1)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A. For example, the specific compound T1.1.13 is thecompound of the formula T1, in which each of the variables R₁, R₂, R₅and R₆ has the specific meaning given in the line A.1.13 of Table A:

According to the same system, also all of the other 1201 specificcompounds disclosed in the Table 1 as well as all of the specificcompounds disclosed in the Tables 2 to T151 are specified analogously.

TABLE 2 This table discloses the 1201 compounds T2.1.1 to T2.1.1201 ofthe formula (T2)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 3 This table discloses the 1201 compounds T3.1.1 to T3.1.1201 ofthe formula (T3)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 4 This table discloses the 1201 compounds T4.1.1 to T4.1.1201 ofthe formula (T4)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 5 This table discloses the 1201 compounds T5.1.1 to T5.1.1201 ofthe formula (T5)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 6 This table discloses the 1201 compounds T6.1.1 to T6.1.1201 ofthe formula (T6)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 7 This table discloses the 1201 compounds T7.1.1 to T7.1.1201 ofthe formula

(T7)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 8 This table discloses the 1201 compounds T8.1.1 to T8.1.1201 ofthe formula

(T8)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 9 This table discloses the 1201 compounds T9.1.1 to T9.1.1201 ofthe formula

(T9)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 10 This table discloses the 1201 compounds T10.1.1 to T10.1.1201of the formula

(T10)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 11 This table discloses the 1201 compounds T11.1.1 to T11.1.1201of the formula

(T11)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 12 This table discloses the 1201 compounds T12.1.1 to T12.1.1201of the formula

(T12)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 13 This table discloses the 1201 compounds T13.1.1 to T13.1.1201of the formula

(T13)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 14 This table discloses the 1201 compounds T14.1.1 to T14.1.1201of the formula

(T14)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 15 This table discloses the 1201 compounds T15.1.1 to T15.1.1201of the formula

(T15)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 16 This table discloses the 1201 compounds T16.1.1 to T16.1.1201of the formula

(T16)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 17 This table discloses the 1201 compounds T17.1.1 to T17.1.1201of the formula

(T17)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 18 This table discloses the 1201 compounds T18.1.1 to T18.1.1201of the formula

(T18)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 19 This table discloses the 1201 compounds T19.1.1 to T19.1.1201of the formula

(T19)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 20 This table discloses the 1201 compounds T20.1.1 to T20.1.1201of the formula

(T20)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 21 This table discloses the 1201 compounds T21.1.1 to T21.1.1201of the formula

(T21)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 22 This table discloses the 1201 compounds T22.1.1 to T22.1.1201of the formula (T22)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 23 This table discloses the 1201 compounds T23.1.1 to T23.1.1201of the formula (T23)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 24 This table discloses the 1201 compounds T24.1.1 to T24.1.1201of the formula (T24)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 25 This table discloses the 1201 compounds T25.1.1 to T25.1.1201of the formula (T25)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 26 This table discloses the 1201 compounds T26.1.1 to T26.1.1201of the formula (T26)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 27 This table discloses the 1201 compounds T27.1.1 to T27.1.1201of the formula (T27)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 28 This table discloses the 1201 compounds T28.1.1 to T28.1.1201of the formula (T28)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 29 This table discloses the 1201 compounds T29.1.1 to T29.1.1201of the formula (T29)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 30 This table discloses the 1201 compounds T30.1.1 to T30.1.1201of the formula (T30)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 31 This table discloses the 1201 compounds T31.1.1 to T31.1.1201of the formula (T31)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 32 This table discloses the 1201 compounds T32.1.1 to T32.1.1201of the formula (T32)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 33 This table discloses the 1201 compounds T33.1.1 to T33.1.1201of the formula (T33)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 34 This table discloses the 1201 compounds T34.1.1 to T34.1.1201of the formula (T34)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 35 This table discloses the 1201 compounds T35.1.1 to T35.1.1201of the formula (T35)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 36 This table discloses the 1201 compounds T36.1.1 to T36.1.1201of the formula (T36)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 37 This table discloses the 1201 compounds T37.1.1 to T37.1.1201of the formula (T37)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 38 This table discloses the 1201 compounds T38.1.1 to T38.1.1201of the formula (T38)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 39 This table discloses the 1201 compounds T39.1.1 to T39.1.1201of the formula (T39)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 40 This table discloses the 1201 compounds T40.1.1 to T40.1.1201of the formula (T40)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 41 This table discloses the 1201 compounds T41.1.1 to T41.1.1201of the formula (T41)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 42 This table discloses the 1201 compounds T42.1.1 to T42.1.1201of the formula (T42)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 43 This table discloses the 1201 compounds T43.1.1 to T43.1.1201of the formula (T43)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 44 This table discloses the 1201 compounds T44.1.1 to T44.1.1201of the formula (T44)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 45 This table discloses the 1201 compounds T45.1.1 to T45.1.1201of the formula (T45)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 46 This table discloses the 1201 compounds T46.1.1 to T46.1.1201of the formula (T46)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 47 This table discloses the 1201 compounds T47.1.1 to T47.1.1201of the formula (T47)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 48 This table discloses the 1201 compounds T48.1.1 to T48.1.1201of the formula (T48)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 49 This table discloses the 1201 compounds T49.1.1 to T49.1.1201of the formula (T49)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 50 This table discloses the 1201 compounds T50.1.1 to T50.1.1201of the formula (T50)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 51 This table discloses the 1201 compounds T51.1.1 to T51.1.1201of the formula (T51)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 52 This table discloses the 1201 compounds T52.1.1 to T52.1.1201of the formula (T52)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 53 This table discloses the 1201 compounds T53.1.1 to T53.1.1201of the formula (T53)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 54 This table discloses the 1201 compounds T54.1.1 to T54.1.1201of the formula (T54)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 55 This table discloses the 1201 compounds T55.1.1 to T55.1.1201of the formula (T55)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 56 This table discloses the 1201 compounds T56.1.1 to T56.1.1201of the formula (T56)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 57 This table discloses the 1201 compounds T57.1.1 to T57.1.1201of the formula (T57)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 58 This table discloses the 1201 compounds T58.1.1 to T58.1.1201of the formula (T58)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 59 This table discloses the 1201 compounds T59.1.1 to T59.1.1201of the formula (T59)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 60 This table discloses the 1201 compounds T60.1.1 to T60.1.1201of the formula (T60)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 61 This table discloses the 1201 compounds T61.1.1 to T61.1.1201of the formula (T61)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 62 This table discloses the 1201 compounds T62.1.1 to T62.1.1201of the formula (T62)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 63 This table discloses the1201 compounds T63.1.1 to T63.1.1201 ofthe formula (T63)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 64 This table discloses the 1201 compounds T64.1.1 to T64.1.1201of the formula (T64)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 65 This table discloses the 1201 compounds T65.1.1 to T65.1.1201of the formula (T65)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 66 This table discloses the 1201 compounds T66.1.1 to T66.1.1201of the formula (T66)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 67 This table discloses the 1201 compounds T67.1.1 to T67.1.1201of the formula (T67)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 68 This table discloses the 1201 compounds T68.1.1 to T68.1.1201of the formula (T68)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 69 This table discloses the 1201 compounds T69.1.1 to T69.1.1201of the formula (T69)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 70 This table discloses the 1201 compounds T70.1.1 to T70.1.1201of the formula (T70)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 71 This table discloses the 1201 compounds T71.1.1 to T71.1.1201of the formula (T71)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 72 This table discloses the 1201 compounds T72.1.1 to T72.1.1201of the formula (T72)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 73 This table discloses the 1201 compounds T73.1.1 to T73.1.1201of the formula (T73)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 74 This table discloses the 1201 compounds T74.1.1 to T74.1.1201of the formula (T74)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 75 This table discloses the 1201 compounds T75.1.1 to T75.1.1201of the formula (T75)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 76 This table discloses the 1201 compounds T76.1.1 to T76.1.1201of the formula

(T76)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 77 This table discloses the 1201 compounds T77.1.1 to T77.1.1201of the formula

(T77)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 78 This table discloses the 1201 compounds T78.1.1 to T78.1.1201of the formula

(T78)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 79 This table discloses the 1201 compounds T79.1.1 to T79.1.1201of the formula

(T79)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 80 This table discloses the 1201 compounds T80.1.1 to T80.1.1201of the formula

(T80)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 81 This table discloses the 1201 compounds T81.1.1 to T81.1.1201of the formula

(T81)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 82 This table discloses the 1201 compounds T82.1.1 to T82.1.1201of the formula

(T82)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 83 This table discloses the 1201 compounds T83.1.1 to T83.1.1201of the formula

(T83)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 84 This table discloses the 1201 compounds T84.1.1 to T84.1.1201of the formula

(T84)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 85 This table discloses the 1201 compounds T85.1.1 to T85.1.1201of the formula

(T85)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 86 This table discloses the 1201 compounds T86.1.1 to T86.1.1201of the formula

(T86)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 87 This table discloses the 1201 compounds T87.1.1 to T87.1.1201of the formula

(T87)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 88 This table discloses the 1201 compounds T88.1.1 to T88.1.1201of the formula

(T88)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 89 This table discloses the 1201 compounds T89.1.1 to T89.1.1201of the formula

(T89)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 90 This table discloses the 1201 compounds T90.1.1 to T90.1.1201of the formula

(T90)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 91 This table discloses the 1201 compounds T91.1.1 to T91.1.1201of the formula (T91)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 92 This table discloses the 1201 compounds T92.1.1 to T92.1.1201of the formula (T92)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 93 This table discloses the 1201 compounds T93.1.1 to T93.1.1201of the formula (T93)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 94 This table discloses the 1201 compounds T94.1.1 to T94.1.1201of the formula (T94)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 95 This table discloses the 1201 compounds T95.1.1 to T95.1.1201of the formula (T95)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 96 This table discloses the 1201 compounds T96.1.1 to T96.1.1201of the formula (T96)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 97 This table discloses the 1201 compounds T97.1.1 to T97.1.1201of the formula (T97)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 98 This table discloses the 1201compounds T98.1.1 to T98.1.1201 ofthe formula (T98)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 99 This table discloses the 1201 compounds T99.1.1 to T99.1.1201of the formula (T99)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 100 This table discloses the 1201 compounds T100.1.1 toT100.1.1201 of the formula (T100)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 101 This table discloses the 1201 compounds T101.1.1 toT101.1.1201 of the formula (T101)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 102 This table discloses the 1201compounds T102.1.1 to T102.1.1201of the formula (T102)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 103 This table discloses the 1201 compounds T103.1.1 toT103.1.1201 of the formula (T103)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 104 This table discloses the 1201 compounds T104.1.1 toT104.1.1201 of the formula (T104)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 105 This table discloses the 1201 compounds T105.1.1 toT105.1.1201 of the formula (T105)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 106 This table discloses the 1201 compounds T106.1.1 toT106.1.1201 of the formula (T106)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 107 This table discloses the 1201 compounds T107.1.1 toT107.1.1201 of the formula (T107)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 108 This table discloses the 1201 compounds T108.1.1 toT108.1.1201 of the formula (T108)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 109 This table discloses the 1201 compounds T109.1.1 toT109.1.1201 of the formula (T109)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 110 This table discloses the 1201 compounds T110.1.1 toT110.1.1201 of the formula (T110)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 111 This table discloses the 1201 compounds T111.1.1 toT111.1.1201 of the formula (T111)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 112 This table discloses the 1201 compounds T112.1.1 toT112.1.1201 of the formula (T112)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 113 This table discloses the 1201 compounds T113.1.1 toT113.1.1201 of the formula (T113)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 114 This table discloses the 1201 compounds T114.1.1 toT114.1.1201 of the formula (T114)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 115 This table discloses the 1201 compounds T115.1.1 toT115.1.1201 of the formula (T115)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 116 This table discloses the 1201 compounds T116.1.1 toT116.1.1201 of the formula (T116)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 117 This table discloses the 1201 compounds T117.1.1 toT117.1.1201 of the formula (T117)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 118 This table discloses the 1201 compounds T118.1.1 toT118.1.1201 of the formula (T118)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 119 This table discloses the 1201 compounds T119.1.1 toT119.1.1201 of the formula (T119)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 120 This table discloses the 1201 compounds T120.1.1 toT120.1.1201 of the formula (T120)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 121 This table discloses the 1201 compounds T121.1.1 toT121.1.1201 of the formula (T121)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 122 This table discloses the 1201 compounds T122.1.1 toT122.1.1201 of the formula (T122)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 123 This table discloses the 1201 compounds T123.1.1 toT123.1.1201 of the formula (T123)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 124 This table discloses the 1201 compounds T124.1.1 toT124.1.1201 of the formula (T124)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 125 This table discloses the 1201 compounds T125.1.1 toT125.1.1201 of the formula (T125)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 126 This table discloses the 1201 compounds T126.1.1 toT126.1.1201 of the formula (T126)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 127 This table discloses the 1201 compounds T127.1.1 toT127.1.1201 of the formula (T127)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 128 This table discloses the 1201 compounds T128.1.1 toT128.1.1201 of the formula (T128)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 129 This table discloses the 1201 compounds T129.1.1 toT129.1.1201 of the formula (T129)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 130 This table discloses the 1201 compounds T130.1.1 toT130.1.1201 of the formula (T130)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 131 This table discloses the 1201 compounds T131.1.1 toT131.1.1201 of the formula (T131)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 132 This table discloses the 1201 compounds T132.1.1 toT132.1.1201 of the formula (T132)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 133 This table discloses the 1201 compounds T133.1.1 toT133.1.1201 of the formula (T133)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 134 This table discloses the 1201 compounds T134.1.1 toT134.1.1201 of the formula (T134)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 135 This table discloses the 1201 compounds T135.1.1 toT135.1.1201 of the formula (T135)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 136 This table discloses the 1201 compounds T136.1.1 toT136.1.1201 of the formula (T136)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 137 This table discloses the 1201 compounds T137.1.1 toT137.1.1201 of the formula (T137)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 138 This table discloses the 1201 compounds T138.1.1 toT138.1.1201 of the formula (T138)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 139 This table discloses the 1201 compounds T139.1.1 toT139.1.1201 of the formula (T139)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 140 This table discloses the 1201 compounds T140.1.1 toT140.1.1201 of the formula (T140)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 141 This table discloses the 1201 compounds T141.1.1 toT141.1.1201 of the formula (T141)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 142 This table discloses the 1201 compounds T142.1.1 toT142.1.1201 of the formula (T142)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 143 This table discloses the 1201 compounds T143.1.1 toT143.1.1201 of the formula (T143)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 144 This table discloses the 1201 compounds T144.1.1 toT144.1.1201 of the formula (T144)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 145 This table discloses the 1201 compounds T145.1.1 toT145.1.1201 of the formula (T145)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 146 This table discloses the 1201 compounds T146.1.1 toT146.1.1201 of the formula (T146)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 147 This table discloses the 1201 compounds T147.1.1 toT147.1.1201 of the formula (T147)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 148 This table discloses the 1201 compounds T148.1.1 toT148.1.1201 of the formula (T148)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 149 This table discloses the 1201 compounds T149.1.1 toT149.1.1201 of the formula (T149)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 150 This table discloses the 1201 compounds T150.1.1 toT150.1.1201 of the formula (T150)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 151 This table discloses the 1201 compounds T151.1.1 toT151.1.1201 of the formula (T151)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 152 This table discloses the 1201 compounds T152.1.1 toT152.1.1201 of the formula (T152)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 153 This table discloses the 1201 compounds T153.1.1 toT153.1.1201 of the formula (T153)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 154 This table discloses the 1201 compounds T154.1.1 toT154.1.1201 of the formula (T154)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 155 This table discloses the 1201 compounds T155.1.1 toT155.1.1201 of the formula (T155)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 156 This table discloses the 1201 compounds T156.1.1 toT156.1.1201 of the formula (T156)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 157 This table discloses the 1201 compounds T157.1.1 toT157.1.1201 of the formula (T157)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 158 This table discloses the 1201 compounds T158.1.1 toT158.1.1201 of the formula (T158)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 159 This table discloses the 1201 compounds T159.1.1 toT159.1.1201 of the formula (T159)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 160 This table discloses the 1201 compounds T160.1.1 toT160.1.1201 of the formula (T160)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 161 This table discloses the 1201 compounds T161.1.1 toT161.1.1201 of the formula (T161)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 162 This table discloses the 1201 compounds T162.1.1 toT162.1.1201 of the formula (T162)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 163 This table discloses the 1201 compounds T163.1.1 toT163.1.1201 of the formula (T163)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

TABLE 164 This table discloses the 1201 compounds T164.1.1 toT164.1.1201 of the formula (T164)

in which, for each of these 1201 specific compounds, each of thevariables R₁, R₂, R₅ and R₆ has the specific meaning given in thecorresponding line, appropriately selected from the 1201 lines A.1.1 toA.1.1201 of Table A.

In further embodiments the invention provides novel intermediates toprovide compounds according to formula (I) are compounds of formula (IV)

wherein R₁₀₀ is wherein R₁₀₀ is halogen, SH, C₁-C₄-alkylthio,C₁-C₄-alkylsulfinyl, C₁-C₄-alkylsulfonyl and R₁, R₂, R₃, R₄, R₆ and R₇are as described herein for compounds of formula (I).

The Following Table Provides a Selection of Compounds of Formula (IV)

R.01

R.02

Mp: 168-170° C. R.03

R.04

R.05

R.06

R.07

R.08

R.09

R.10

R.11

R.12

Mp:  85-87° C. R.13

R.14

R.15

R.16

R.17

R.18

R.19

R.20

R.21

R.22

Oil; (M + 1)⁺ 300 R.23

R.24

R.25

R.26

R.27

R.28

R.29

R.30

R.31

R.32

Oil; (M + 1)⁺ 290 R.33

R.34

R.35

R.36

R.37

R.38

R.39

R.40

R.41

R.42

R.43

R.44

R.45

R.46

R.47

R.48

R.49

R.50

R.51

R.52

R.53

R.54

R.55

R.56

R.57

R.58

R.59

R.60

The active compounds of component B are known e.g. from the PesticideManual (British Crop Protection Council).N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamidehas the Chemical Abstracts Registry Number [1072957-71-1]. The compoundof formula (II) has the Chemical Abstracts Registry Number[173662-97-0]. The compounds(S)-[3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)isoxazol-4-yl]pyridin-3-yl-methanol,3-(4-Chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)isoxazol-4-yl]pyridin-3-yl-methanolare found in WO2010069881.

The active ingredient mixture of the compounds of formula I selectedfrom tables T1 to T164 or a specific compound selected from P.1 to P.372with active ingredients described above comprises a compound selectedfrom tables T1 to T164 and an active ingredient as described abovepreferably in a mixing ratio of from 100:1 to 1:6000, especially from50:1 to 1:500, more especially in a ratio of from 20:1 to 1:200, evenmore especially from 10:1 to 1:100, very especially from 5:1 and 1:50,special preference being given to a ratio of from 3:1 to 1:10, and aratio of from 3:1 to 1:5 being likewise preferred, above all in a ratioof 1:1, or 5:1, or 5:2, or 5:3, or 5:4, or 4:1, or 4:2, or 4:3, or 3:1,or 3:2, or 2:1, or 1:5, or 2:5, or 3:5, or 4:5, or 1:4, or 2:4, or 3:4,or 1:3, or 2:3, or 1:2, or 1:600, or 1:300, or 1:150, or 1:35, or 2:35,or 4:35, or 1:75, or 2:75, or 4:75, or 1:6000, or 1:3000, or 1:1500, or1:350, or 2:350, or 4:350, or 1:750, or 2:750, or 4:750. Those mixingratios are understood to include, on the one hand, ratios by weight andalso, on other hand, molar ratios.

The mixtures comprising a compound of formula I e.g. selected fromtables T1 to T164 or a specific compound selected from P.1 to P.372 andone or more active ingredients as described above can be applied, forexample, in a single “ready-mix” form, in a combined spray mixturecomposed from separate formulations of the single active ingredientcomponents, such as a “tank-mix”, and in a combined use of the singleactive ingredients when applied in a sequential manner, i.e. one afterthe other with a reasonably short period, such as a few hours or days.The order of applying the compounds of formula I e.g. those selectedfrom tables T1 to T164 and the active ingredients as described above isnot essential for working the present invention.

A synergistic effect exists whenever the action of an active ingredientcombination is greater than the sum of the actions of the individualcomponents.

The action to be expected E for a given active ingredient combinationobeys the so-called COLBY formula and can be calculated as follows(COLBY, S. R. “Calculating synergistic and antagonistic responses ofherbicide combination”. Weeds, Vol. 15, pages 20-22; 1967):

ppm=milligrams of active ingredient (=a.i.) per liter of spray mixture

X=% action by active ingredient A) using p ppm of active ingredient

Y=% action by active ingredient B) using q ppm of active ingredient.According to COLBY, the expected (additive) action of active ingredientsA)+B) using p+q ppm of active ingredient is

$E = {X + Y - \frac{X \cdot Y}{100}}$

If the action actually observed (O) is greater than the expected action(E), then the action of the combination is super-additive, i.e. there isa synergistic effect. In mathematical terms the synergism factor SFcorresponds to O/E. In the agricultural practice an SF of ≧1.2 indicatessignificant improvement over the purely complementary addition ofactivities (expected activity), while an SF of ≦0.9 in the practicalapplication routine signals a loss of activity compared to the expectedactivity.

EXAMPLES Preparation of 1-(3,5-difluorophenyl)ethanol

To a colorless stirred solution of ^(3′),^(5′)-difluoroacetophenone(50.00 g, 320.24 mmol) in methanol (320 mL), sodium borohydride (3.41 g,86.47 mmol, 0.27 eq) was added portion wise over 20 minutes at roomtemperature under inert atmosphere (Ar). Then the reaction mixture wasstirred for 45 min at room temperature and then quenched carefully bythe addition of a saturated aqueous ammonium chloride solution (150 mL).The extraction was carried out with ethyl acetate (2×200 mL). Thecombined organic layers were washed with brine (200 mL), dried overanhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to givethe title compound (50.29 g, 99%) as a colorless oil. The alcohol wasused as such in the subsequent step.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.27.

Preparation of (−)-(S)-1-(3,5-difluorophenyl)ethanol

To a stirred solution of (−)-DIP-Cl ((−)-diisopinocampheylboronchloride) (2.67 g, 8.33 mmol, 1.3 eq) in THF (20 mL) kept under inertatmosphere (Ar) and cooled to −27° C. to −25° C.,^(3′),^(5′)-difluoroacetophenone (1.00 g, 6.40 mmol) was added drop wiseover 2 min. The reaction was maintained at this temperature for 17 h.The reaction mixture was then treated with acetaldehyde (0.44 mL, 7.69mmol, 1.2 eq). Thereafter, the temperature was allowed to reach roomtemperature and the reaction mixture was stirred at for 7 h. The solventwas then removed in vacuo and the resulting residue was partitionedbetween water (10 mL) and TBME (tert-butyl-methyl ether) (20 mL). Theaqueous phase was extracted again with TBME (20 mL). The organic layerwas washed with an aqueous 2 N NaOH solution (20 mL), brine (20 mL),dried over anhydrous Na₂SO₄ and filtered. The solvent was removed invacuo to give a residue, which was purified by two subsequent columnchromatographic steps: First by normal phase chromatography (silica gel,heptane/ethyl acetate, v/v=1/0-9/1) followed by a reversed phasechromatography (90 C₁₈-silica gel, acetonitrile for the second one).This gave the title compound (0.40 g, 40%) as a colorless oil with aspecific rotation of [α]²⁵ _(D)=−26.66 (c=1.054 g/100 mL, CH₂Cl₂, 589nm).

Preparation of cis and trans 4-isopropylcyclohexanol

To a stirred solution of 4-isopropylcyclohexanone (10.00 g, 68.46 mmol)in tert-butyl methyl ether (136 mL) cooled to 7° C. (cooling bath with acyclohexane/liquid nitrogen slurry), a 1.00 M solution of lithiumaluminium hydride in THF (23 mL, 22.59 mmol, 0.33 eq) was added dropwise over 35 minutes while keeping the temperature in the range of 7 to10° C. Stirring was continued under these conditions. The reactionmixture was then allowed to reach room temperature and stirred at thistemperature for an additional 40 minutes. It was then carefully quenchedby the slow addition of water (20 mL), followed by a one molar aqueoussulfuric acid solution (60 mL). The extraction was carried out withtert-butyl methyl ether (2×50 mL). The organic layer was washed with asaturated aqueous Na₂CO₃ solution (80 mL), brine (80 mL), dried overanhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to givea residue, which was purified by column chromatography (silica gel,heptane/ethyl acetate, v/v=1/0−9/1). Fractions containing the purecompounds were collected and concentrated in vacuo to give pure trans(6.91 g, 71%) and the pure cis isomer (0.68 g, 5%) of4-isopropyl-cyclohexanol both as colourless oils.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, detection by spraying with Mo—Ce reagent, eluent:heptanes/ethyl acetate 4:1 (v/v); R_(f) of cis4-isopropylcyclohexanol=0.20); R_(f) of trans4-isopropylcyclohexanol=0.15.

Preparation of3-bromo-2-(cis-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine

To a stirred suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (23.65g, 101.5 mmol) in THF (180 mL), trans isopropylcyclohexanol (14.44 g,101.5 mmol, 1.0 eq) and triphenylphosphine (32.27 g, 121.8 mmol, 1.2 eq)were added at room temperature under inert atmosphere (Ar). To thismixture, DIAD (diisopropyl diazodicarboxylate) (25.51 mL, 121.8 mmol,1.2 eq) was added drop wise over 45 min while keeping the temperaturebelow 45° C. Then, the reaction mixture was stirred for 5 h underheating to reflux. TLC indicated that the starting material wasconsumed. The reaction mixture was therefore allowed to reach roomtemperature and it was quenched by the addition of water (250 mL). Theextraction was carried out with ethyl acetate (3×200 mL). The organiclayer was washed with brine (300 mL), dried over anhydrous Na₂SO₄ andfiltered. The solvent was removed in vacuo to give a residue, which waspurified by column chromatography (silica gel, heptane/ethyl acetate,v/v=1/0-98/2). Fractions containing the pure compound were collected andconcentrated in vacuo to give title compound (22.59 g, 62%) in the formof an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.64.

Preparation of5-bromo-6-(cis-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine

To a stirred solution of3-bromo-2-(cis-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine (22.59g, 63.24 mmol) in EtOH/H₂O (600 mL/150 mL, 4/1 v/v), ammonium chloride(3.45 g, 63.24 mmol, 1.0 eq) and iron powder (14.27 g, 253.0 mmol, 4 eq)were added at room temperature under inert atmosphere (Ar). The reactionmixture was stirred for 3 h under heating to reflux. As TLC indicatedthat the starting material was consumed at this point in time, thereaction mixture was cooled to room temperature and filtered through apad of celite. The resulting filtrate was concentrated in vacuo and theresidue partitioned between a 2 molar aqueous NaOH solution (100 mL) andethyl acetate (150 mL). After phase separation, the aqueous phase wasextracted once more with ethyl acetate (2×100 mL). The organic layer waswashed with brine (400 mL), dried over anhydrous Na₂SO₄ and filtered.The solvent was removed in vacuo to afford the title compound (21.01 g,101%) in the form of an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.19.

Preparation ofN′-[5-bromo-6-(cis-4-isopropylcyclohexoxy)-2-methyl-3-pyridyl]-N-ethyl-N-methylformamidine

The Vilsmeier reagent was freshly prepared by the slow addition ofphosphorus oxychloride (7.09 mL, 75.89 mmol, 1.2 eq) to a solution ofN,N-ethylmethylformamide (6.61 g, 75.89 mmol, 1.2 eq) in dichloromethane(75 mL) at room temperature. After the addition was complete, thereaction mixture was stirred at room temperature for 1 h. The Vilsmeierreagent was then added drop wise over 40 min to a solution of5-bromo-6-(cis-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine (20.70g, 63.24 mmol) in dichloromethane (225 mL) at room temperature underinert atmosphere (Ar). Stirring was continued for 1.5 h at roomtemperature. The reaction mixture was then quenched by the addition ofwater (100 mL) and the pH was adjusted to 14 by the addition of a 2.0molar aqueous NaOH solution (80 mL). The phases were separated and theaqueous phase extracted with dichloromethane (2×100 mL). The organiclayer was washed with brine (250 mL), dried over anhydrous Na₂SO₄ andfiltered. The solvent was removed in vacuo to give a residue, which waspurified by column chromatography (silica gel, heptane/ethyl acetate,v/v=1/0-4/1). Fractions containing the pure compound were collected andconcentrated in vacuo to give the title compound (20.23 g, 81%) as ayellow oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.29.

¹H NMR (400 MHz, CDCl₃): δ (ppm)=7.45-7.30 (broad s, 1H), 7.23 (s, 1H),5.32-5.28 (m, 1H), 3.55-3.24 (broad s, 2H), 2.98 (s, 3H), 2.35 (s, 3H),2.04-2.01 (m, 2H), 1.63-1.46 (m, 7H), 1.20 (t, 3H), 1.18-1.10 (m, 1H),0.91-0.89 (d, 6H).

Preparation of3-bromo-2-(trans-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine

To a stirred suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (2.00g, 8.58 mmol) in THF (8.6 mL), cis isopropylcyclohexanol (1.44 g, 8.58mmol, 1.0 eq) and triphenylphosphine (2.73 g, 10.30 mmol, 1.2 eq) wereadded at room temperature under inert atmosphere (Ar). To this mixture,DIAD (diisopropyl diazodicarboxylate) (2.16 mL, 10.30 mmol, 1.2 eq) wasadded drop wise over 10 minutes while keeping the temperature below 40°C. The reaction mixture was stirred for 1.5 h under heating to. Afterthis point in time, TLC indicted consumption of the starting materialand the reaction mixture was allowed to reach room temperature and wasquenched by adding water (20 mL). The water phase was extracted withethyl acetate (3×20 mL). The organic layer was washed with brine (35mL), dried over anhydrous Na₂SO₄ and filtered. The solvent was removedin vacuo to give a residue, which was purified by column chromatography(silica gel, heptane/ethyl acetate, v/v=1/0-9/1). Fractions containingthe pure compound were collected and concentrated in vacuo to give thetitle compound (0.94 g, 30%) as an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.65.

Preparation of5-bromo-6-(trans-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine

To a stirred solution of3-bromo-2-(trans-4-isopropylcyclohexoxy)-6-methyl-5-nitro-pyridine(0.917 g, 2.00 mmol) in EtOH/H₂O (24 mL/6 mL, 4/1 v/v), ammoniumchloride (0.109 g, 2.00 mmol, 1.0 eq) and iron powder (0.452 g, 8.00mmol, 4 eq) were added at room temperature under inert atmosphere (Ar).The reaction mixture was stirred under heating to reflux for 3 h. Atthis point in time, TLC indicated that the starting material wasconsumed. Therefore, the reaction mixture was allowed to reach roomtemperature and was filtered through a pad of celite. The filtrate wasconcentrated under reduced pressure and the residue partitioned betweena 2 molar aqueous NaOH solution (20 mL) and ethyl acetate (30 mL). Thephases were separated and the aqueous phase extracted with ethyl acetate(2×20 mL). The organic layer was washed with brine (40 mL), dried overanhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo toafford the title compound (0.658 g, 100%) as an oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.19.

Preparation of5-bromo-6-(trans-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine

The Vilsmeier reagent was freshly prepared by the slow addition ofphosphorus oxychloride (0.101 mL, 1.08 mmol, 1.2 eq) to a solution ofN,N-ethylmethylformamide (0.094 g, 1.08 mmol, 1.2 eq) in dichloromethane(0.5 mL) at room temperature. After the addition was complete, thereaction mixture was stirred at room temperature for 1 h. Then theVilsmeier reagent thus obtained was added drop wise to a solution of5-bromo-6-(trans-4-isopropylcyclohexoxy)-2-methyl-pyridin-3-amine (0.295g, 0.90 mmol) in dichloromethane (1.0 mL) at room temperature underinert atmosphere (Ar). Stirring was continued was for 1.5 h at roomtemperature. The reaction was then quenched by the addition of a 2 molaraqueous NaOH solution (5 mL). The phases were separated and the aqueousphase extracted with dichlormethane (2×10 mL). The organic layer waswashed with brine (10 mL), dried over anhydrous Na₂SO₄ and filtered. Thesolvent was removed in vacuo to give a residue, which was purified bycolumn chromatography (silica gel, heptane/ethyl acetate, v/v=1/0-4/1).Fractions containing the pure compound were collected and concentratedin vacuo to give the title compound (0.191 g, 54%) as a light yellowoil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.29.

¹H NMR (400 MHz, CDCl₃): δ (ppm)=7.45-7.30 (broad s, 1H), 7.22 (s, 1H),4.93-4.85 (m, 1H), 3.55-3.22 (broad s, 2H), 2.98 (s, 3H), 2.35 (s, 3H),2.19-2.15 (m, 2H), 1.80-1.77 (m, 2H), 1.50-1.09 (m, 5H), 1.28 (t, 3H),0.88-0.86 (d, 6H).

Preparation of N-Ethyl-N-methyl-formamide

113 g (1.912 mol) of ethylmethylamine was dissolved in 500 mL of drytoluene. 75.86 mL of formic acid (92.2 g, 2.01 mol) was added drop-wiseover 20 minutes. Hereby, an exothermic reaction was observed. Thetemperature was kept below 35° C. by cooling with an ice-water coolingbath. The turbid solution was stirred under heating to reflux (bathtemperature of 175° C.) and the water removed using a Dean and Starkseparator. 46 mL of water phase was thus separated. This water phase wasextracted with 50 mL of ethyl acetate. And this ethyl acetate solutionwas added to the reaction mixture, after this one was allowed to reachroom temperature. After evaporation of the solvent, the resulting liquidwas subjected to a fractionating column distillation (Widmer column) at80 mbar. 138 g of a colourless liquid of bp=95-96° C. was collected. Asthis material was contaminated with formic acid, the liquid was taken upin 1.0 L of ethyl acetate and kept over K₂CO₃ (occasional stirring, 24 hoverall). The solution was then filtered and washed with water and theorganic phase was again subjected to the distillation procedurementioned before. This gave 130.4 g of the title compound as a liquid(bp=95-96° C., 80 mbar).

Preparation of methoxyethylmethyl-methanaminium methyl sulfate

128 g of N-ethyl-N-methyl-formamide was added slowly to 139 mL (185 g,1.469 mol) of dimethyl sulfate (the dimethyl sulfate used was freshlydistilled in vacuo after having been tried over K₂CO₃). The colourlesssolution was warmed under stirring to 50° C. whereupon an exothermicreaction was starting up. The heating bath was removed and the reactionmixture reached a temperature of 86° C. After the exothermicity came toan end, the reaction mixture was stirred at a temperature of 80° C. foran additional 3 hours. Thereafter, the reaction mixture was allowed toreach room temperature. The resulting liquid was then shaken in aseparatory funnel first with 100 mL of toluene and, after phaseseparation, with 100 mL of diethyl ether. Traces of solvents wereremoved in vacuo (rotovapor) to give 294 g of the title compound in theform of a colourless liquid. The compound was used as such in thesubsequent step.

Preparation of5-Bromo-2-methyl-3-nitro-6-[2,2,2-trifluoro-1-(4-fluorophenyl)ethoxy]pyridine

To a stirred suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (0.10g, 0.43 mmol) in THF (3 mL), 2,2,2-trifluoro-1-(4-fluorophenyl)ethanol(0.13 g, 0.64 mmol, 1.5 equiv) and triphenylphosphine (0.17 g, 0.64mmol, 1.5 eq) were added at room temperature under inert atmosphere(Ar). To this mixture, DIAD (diisopropyl diazodicarboxylate) (0.13 mL,0.64 mmol, 1.5 eq) was added dropwise over 10 minutes while keeping thetemperature below 40° C. The reaction mixture was stirred for 6 h underheating at 60° C. After this time, TLC indicted that the startingmaterial had been consumed and the reaction mixture was allowed to reachroom temperature before quenching with water (10 mL). The water phasewas extracted with ethyl acetate (3×15 mL). The organic layer was washedwith brine (20 mL), dried over anhydrous Na₂SO₄ and filtered. Thesolvent was removed in vacuo to give a brown residue, which was purifiedby combiflash column chromatography (silica gel, heptane/ethyl acetate,v/v=95/5). Fractions containing the pure compound were collected andconcentrated in vacuo to give the title compound (0.11 g, 62% yield) asa yellow oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 4:1 (v/v);R_(f) of the title compound=0.65.

Preparation of 2,2,2-Trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol

In a 50 mL two-neck flask,2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanone (2.0 g, 8.3 mmol)was dissolved in methanol (8 mL) and sodium borohydride (0.31 g, 8.3mmol) was added carefully in portions with ice-bath cooling. Theresultant colourless solution was stirred at RT for 2 hours andmonitored by TLC. Upon the disappearance of all starting material, 5 mLof an aqueous saturated NH₄Cl solution was slowly added to the reactionmixture with additional stirring for 10 min. The later was extracted 3times with 20 mL of EtOAc and the organic fractions were combined andwashed with 10 mL of brine, dried over Na₂SO₄, and filtered. The solventwas removed under reduced pressure to give2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol (2.13 g,quantitative) as a colourless oil which was used with no furtherpurification.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 2:1 (v/v);R_(f) of the title compound=0.50.

Preparation of5-Bromo-2-methyl-3-nitro-6-[2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethoxy]pyridine

To a stirring suspension of 3-bromo-6-methyl-5-nitro-pyridin-2-ol (0.25g, 1.07 mmol) in THF (7 mL),2,2,2-trifluoro-1-[4-(trifluoromethyl)phenyl]ethanol (0.39 g, 1.61 mmol,1.5 equiv) and triphenylphosphine (0.42 g, 1.61 mmol, 1.5 eq) were addedat room temperature under inert atmosphere (Ar). To this mixture, DIAD(diisopropyl diazodicarboxylate) (0.33 mL, 1.61 mmol, 1.5 eq) was addeddropwise over 10 minutes while keeping the temperature below 40° C. Thereaction mixture was stirred for 6 h under heating at 60° C. After thistime, TLC indicted that the starting material was consumed and thereaction mixture was allowed to reach room temperature before quenchingwith water (10 mL). The water phase was extracted with ethyl acetate(2×50 mL). The organic layer was washed with brine (20 mL), dried overanhydrous Na₂SO₄ and filtered. The solvent was removed in vacuo to givea brown residue, which was purified by combiflash column chromatography(silica gel, heptane/ethyl acetate, v/v=95/5). Fractions containing thepure compound were collected and concentrated in vacuo to give the titlecompound (0.18 g, 41% yield) as a yellow oil.

TLC: Plates: Merck TLC-Plates, silica gel F₂₅₄, saturated atmosphere indeveloping tank, UV detection, eluent: heptanes/ethyl acetate 2:1 (v/v);R_(f) of the title compound=0.74.

Preparation of 1,1,1-Trifluorohept-6-en-2-ol

To a ice-bath cooled solution of hex-5-enal (500 mg, 4.331 mmol) andtrimethyl(trifluoromethyl)silane (0.74 g, 5.13 mmol, 1.2 equiv.) in THF(10 mL) was added tetrabutylammonium hydrofluoride (10 mg, 0.04 mmol).The ice bath was removed and the reaction progress was monitored viaGCMS and 1H NMR. Upon complete transformation of the starting materialthe reaction mixture was treated with 2M HCl and stirred for anadditional 2 h. Then, 50 mL of Et₂O was introduced and the layers wereseparated. The aqueous fraction was additionally extracted with Et₂O andthe combined organic phases were washed sequentially with a saturatedaqueous NaHCO₃ solution, water, and brine. After drying with MgSO₄ andfiltration the solvent was removed under reduced pressure and theresultant crude residue was purified by column chromatography (silicagel, pentane/Et₂O, v/v=8/2). Fractions containing the pure compound werecollected and concentrated in vacuo to give1,1,1-trifluorohept-6-en-2-ol (225 mg, 31% yield) as a yellow oil.

Using techniques analogous to those above and further techniques knownto the person skilled in the art, for example as found in WO 08/101,682,the compounds found in Table Q were prepared.

TABLE Q LC-Method: R_(t) (min); MS-ESI (m/z; (M + H)⁺) Q.001

Method 4: 1.42 min; 370 Q.002

Method 4: . 1.46 min; 358 Q.003

Method 4: 1.30 min; 328 Q.004

Method 4: 1.33 min; 342 Q.005

Method 4: 1.17 min; 398 Q.006

Gum Q.007

Method 4: 1.32 min; 292 Q.008

Method 4: 1.39 min; 356 Q.009

Mp 72-73° C. Q.010

Method 4: 1.42 min; 356 Q.011

Gum Q.012

Gum Q.013

Gum Q.014

Gum Q.015

Gum Q.016

Gum Q.017

Gum Q.018

Gum Q.019

Gum Q.020

Gum Q.021

Gum Q.022

Gum Q.023

Gum Q.024

Gum Q.025

Gum Q.026

Gum Q.027

Gum Q.028

Method 4: 1.32 min; 418 Q.029

Liquid Q.030

Method 4: 1.53 min; 544 Q.031

Gum Q.032

Liquid Q.033

Method 4: 1.31 min; 444 Q.034

Method 4: 1.22 min; 340 Q.035

Method 4: 0.99 min; 358 Q.036

Method 4: 0.98 min; 388 Q.037

Solid Q.038

Liquid Q.039

Method 4: 1.48 min; 473 Q.040

Liquid Q.041

Liquid Q.042

Liquid Q.043

Liquid Q.044

Method 4: 1.28 min; 446 Q.045

Gum Q.046

Gum Q.047

Gum Q.048

Gum Q.049

Gum Q.050

Gum Q.051

Liquid Q.052

Method 4: 1.18 min; 360 Q.053

Liquid Q.054

Liquid Q.055

Liquid Q.056

Solid Q.057

Method 4: 1.19 min; 276 Q.058

Method 4: 1.64 min; 348 Q.059

Method 4: 1.00 min; 392 Q.060

Method 4: 1.16 min; 420 Q.061

Liquid Q.062

Method 4: 1.34 min; 388 Q.063

Method 4: 1.16 min; 338 Q.064

Mp 77-78° C. Q.065

Liquid Q.066

Liquid Q.067

Liquid Q.068

Solid Q.069

Method 4: 1.30 min; 410 Q.070

Liquid Q.071

Gum Q.072

Solid Q.073

Solid Q.074

Liquid Q.075

Liquid Q.076

Liquid Q.077

Liquid Q.078

Liquid Q.079

Method 4: 1.39 min; 368 Q.080

Liquid Q.081

Liquid Q.082

Liquid Q.083

Liquid Q.84

Liquid Q.085

Gum Q.086

Liquid Q.087

Liquid Q.088

Liquid Q.089

Liquid Q.090

Liquid Q.091

Liquid Q.092

Liquid Q.093

Gum Q.094

Liquid Q.095

Method 1: 13.577 min; 362 Q.096

Mp 81-82° C. Q.097

Method 2: 11.956 min; 398 Q.098

Method 1: 11.773 min; 352 Q.099

Method 1: 11.755 min; 376 Q.100

Method 1: 12.320 min; 390 Q.101

Method 1: 12.207 min; 440 Q.102

Method 1: 11.873 min; 376 Q.103

Method 1: 13.153 min; 382 Q.104

Method 1: 6.418 min; 438 Q.105

Method 1: 11.571 min; 400 Q.106

Method 1: 12.115 min; 365 Q.107

Mp 107-108° C. Q.108

Method 2: 12.713 min; 523 Q.109

Method 1: 12.881 min; 479 Q.110

Method 2: 12.214 min; 402 Q.111

Mp 57-59° C. Q.112

Method 2: 12.236 min; 390 Q.113

Method 1: 12.030 min; 412 Q.114

Method 2: 13.002 min; 404 Q.115

Method 1: 9.589 min; 393 Q.116

Method 2: 11.625 min; 394 Q.117

Method 2: 6.956 min; 377 Q.118

Method 2: 12.577 min; 368 Q.119

Method 1: 13.850 min; 444 Q.120

Method 2: 11.861 min; 354 Q.121

Method 2: 12.977 min; 451 Q.122

Method 2 13.353 min; 394 Q.123

Mp 120-121° C. Q.124

Mp 98-99° C. Q.125

Mp 101-102° C. Q.126

Method 1: 13.029 min; 480 Q.127

Method 2: 13.168 min; 481 Q.128

Mp 60-62° C. Q.129

Mp 46-48° C. Q.130

Method 2: 3.41 min; 377 Q.131

Method 2: 12.242 min; 408 Q.132

Method 1: 12.688 min; 368 Q.133

Method 1: 12.522 min; 368 Q.134

Method 2: 12.979 min; 380 Q.135

Method 3: 1.49 min; 396: Cis Q.136

Method 1: 10.914 min; 431 Q.137

Mp 43-45° C. Q.138

Method 1: 13.065 min; 402 Q.139

Method 1: 13.387 min; 370 Q.140

Method 2: 12.176 min; 366 Q.141

Method 1: 12.712 min; 368 Q.142

Method 1: 13.557 min; 466 Q.143

Mp 71-73° C. Q.144

Method 1: 11.879 min; 503 Q.145

Mp 106-107° C. Q.146

Method 1: 11.862 min; 344 Q.147

Method 1: 12.605 min; 404 Q.148

Method 1: 12.704 min; 405 Q.149

Method 1: 12.642 min; 370 Q.150

Method 1: 13.317 min; 372 Q.151

Liquid Q.152

Mp 100-101° C. Q.153

Mp 43-44° C. Q.154

Mp 53-57° C. Q.155

Mp 75-78° C. Q.156

Mp 90-91° C. Q.157

Mp 125-127° C. Q.158

Liquid Q.159

Liquid Q.160

Liquid Q.161

Liquid Q.162

Liquid Q.163

Mp 90-95° C. Q.164

Mp 88-90° C. Q.165

Liquid Q.166

Liquid Q.167

Liquid Q.168

Liquid Q.169

Liquid Q.170

Liquid Q.171

Liquid Q.172

Mp 72-76° C. Q.173

Liquid Q.174

Liquid Q.175

Liquid Q.176

Liquid Q.177

Liquid Q.178

Method 2: 12.011 min; 460 Q.179

Method 1: 13.777 min; 444; Trans Q.180

Method 1: 13.653 min; 444; Cis Q.181

Method 2: 11.260 min; 334 Q.182

Method 1: 13.163 min; 318; Trans Q.183

Method 1: 14.926 min; 318; Cis Q.184

Method 2: 12.116 min; 348 Q.185

Method 1: 14.254 min; 332; Trans Q.186

Method 1: 15.845 min; 332; Cis Q.187

Method 2: 12.707 min; 426 Q.188

Method 2: 12.145 min; 426 Q.189

Method 2: 11.943 min; 422 Q.190

Method 1: 12.216 min; 436 Q.191

Method 2: 12.769 min; 426 Q.192

Method 2: 12.121 min; 424 Q.193

Method 2: 11.891 min; 424 Q.194

Method 2: 11.881 min; 422 Q.195

Mp 52-54° C. Q.196

Method 1: 12.439 min; 466 Q.197

Method 1: 11.886 min; 416 Q.198

Method 1: 11.886 min; 390 Q.199

Method 1: 11.955 min; 418 Q.200

Method 1: 12.096 min; 402 Q.201

Method 1: 12.796 min; 418 Q.202

Method 1: 12.154 min; 496 Q.203

Method 2: 13.148 min; 404 Q.204

Method 2: 11.780 min; 412 Q.205

Method 1: 6.785 min; 444 Q.206

Mp 75-78° C. Q.207

Mp 57-58° C. Q.208

Method 1: 10.753 min; 368 Q.209

Method 1: 7.472 min; 413 Q.210

Mp 134-135° C. Q.211

Method 1: 11.913 min; 440 Q.212

Method 1: 11.392 min; 410 Q.213

Method 1: 8.301 min; 370 Q.214

Method 1: 11.318 min; 364 Q.215

Method 1: 12.017 min; 384 Q.216

Method 2: 12.660 min; 374 Q.217

Method 1: 12.015 min; 426 Q.218

Method 2: 12.403 min; 408 Q.219

Method 2: 13.469 min; 418 Q.220

Method 1: 11.837 min; 354 Q.221

Method 1: 13.221 min; 458 Q.222

Method 2: 11.427 min; 340 Q.223

Method 1: 12.006 min; 390 Q.224

Method 2: 12.567 min; 416 Q.225

Method 2: 13.408 min; 430 Q.226

Method 1: 12.686 min; 416 Q.227

Method 2: 13.431 min; 430 Q.228

Method 2: 12.346 min; 362 Q.229

Method 2: 11.570 min; 358 Q.230

Method 1: 12.261 min; 372 Q.231

Method 1: 13.535 min; 394 Q.232

Method 1: 13.295 min; 394 Q.233

Method 2: 11.937 min; 422 Q.234

Method 1: 14.173 min; 398 Q.235

Mp 55-57° C. Q.236

Mp 40-42° C. Q.237

Method 1: 8.524 min; 382 Q.238

Method 1: 19.177 min; 430 Q.239

Method 1: 18.583 min; 416 Q.240

Method 1: 10.070 min; 447 Q.241

Method 1: 12.850 min; 446 Q.242

Method 1: 8.079 min; 427 Q.243

Method 1: 12.200 min; 402 Q.244

Method 1: 9.090 min; 356 Q.245

Method 1: 8.672 min; 382 Q.246

Method 1: 11.718 min; 383 Q.247

Method 1: 13.430 min; 368; Cis Q.248

Method 1: 13.051 min; 348; Cis Q.249

Method 1: 14.416 min; 358; Cis Q.250

Method 1: 13.413 min; 342; Cis Q.251

Method 1; 14.420 min; 346; Cis Q.252

Method 1: 13.397 min; 346; Trans Q.253

Method 2: 13.397 min; 342; Trans Q.254

Method 1: 13.900 min; 356 Q.255

Mp 178-180° C. Q.256

Mp 165-168° C. Q.257

Method 3: 1.42 min; 370 Q.258

Method 3: 1.55 min; 412 Q.259

Method 3: 1.68 min; 454 Q.260

Method 3: 1.34 min; 412; (S) Q.261

Method 3: 1.34 min; 412; (R) Q.262

Ionic liquid Q.263

Method 3: 1.41 min; 410 Q.264

Method 3: 1.42 min; 428 Q.265

Method 3 1.40 min; 416 Q.266

Method 3: 1.21 min; 411 Q.267

Method 3: 1.55 min: 452 Q.268

Method 3: 1.52 min; 396; Trans Q.269

Method 3: 1.43 min: 430; Cis Q.270

Mp 111-113° C.; Trans Q.271

Method 1: 13.010 min; 372 Q.272

Method 1: 11.512 min; 386 Q.273

Method 1: 14.147 min; 400 Q.274

Method 1: 14.704 min; 414 Q.275

Method 1: 12.441 min; 388 Q.276

Method 1: 12.949 min; 402 Q.277

Method 1: 12.412 min; 388 Q.278

Method 1: 12.930 min; 402 Q.279

Method 1: 11.765 min; 390 Q.280

Method 1: 13.223 min; 376 Q.281

Method 1: 9.144 min; 366 Q.282

Method 1: 9.411 min; 380 Q.283

Method 1: 13.076 min; 404 Q.284

Method 1: 13.397 min; 404 Q.285

Method 1: 12.345 min; 390 Q.286

Method 1: 12.464 min; 390 Q.287

Method 1: 13.376 min; 418 Q.288

Method 2: 12.056 min; 354 Q.289

Method 1: 11.736 min; 412 Q.290

Mp 81-85° C. Q.291

Method 1: 11.782 min; 408 Q.292

Method 1: 12.318 min; 422 Q.293

Method 1: 12.503 min; 366 Q.294

Method 1: 13.526 min; 438 Q.295

Mp 59-62° C. Q.296

Method 1: 11.641 min; 312 Q.297

Method 1: 11.974 min; 326 Q.298

Mp 57-61° C. Q.299

Method 1: 12.313 min; 394 Q.300

Mp 53-56° C. Q.301

Method 1: 12.908 min; 410 Q.302

Method 1: 12.267 min; 440 Q.303

Method 1: 12.897 min; 454 Q.304

Mp 82-86° C. Q.305

Mp 77-81° C. Q.306

Method 1: 12.789 min; 404 Q.307

Method 1: 13.266 min; 418 Q.308

Method 1: 13.998 min; 396 Q.309

Method 1: 13.324 min; 466 Q.310

Method 1: 13.568 min; 462 Q.311

Method 1: 13.806 min; 462 Q.312

Method 1: 14.266 min; 476 Q.313

Method 1: 14.120 min; 476 Q.314

Method 1: 14.042 min; 480 Q.315

Method 1: 12.395 min; 366 Q.316

Method 1: 7.382 min; 352 Q.317

Mp 78-81° C. Q.318

Method 1: 12.537 min; 430 Q.319

Method 1: 13.594 min; 416 Q.320

Mp 27-30° C. Q.321

Method 1: 12.591 min; 390 Q.322

Mp 67-68° C. Q.323

Mp 83-84° C. Q.324

Method 1: 12.813 min; 390 Q.325

Mp 56-57° C. Q.326

Mp 61-62° C. Q.327

Method 1: 13.121 min; 426 Q.328

Liquid Q.329

Method 1: 14.077 min; 480 Q.330

Method 1: 11.439 min; 392 Q.331

Method 1: 11.711 min; 340 Q.332

Method 1: 9.781 min; 382; Isomer 1 Q.333

Method 1: 9.758 min; 382 Isomer 2 Q.334

Method 6: 0.92 min; 396 Q.335

Method 1: 11.804 min; 408 Q.336

Method 1: 8.965 min; 424 Q.337

Mp 104-108° C. Q.338

Method 1: 10.918 min; 331 Q.339

Method 1: 11.312 min; 344 Q.340

Method 1: 12.292 min; 366 Q.341

Method 1: 11.200 min; 290 Q.342

Method 1: 11.930 min; 304 Q.343

Method 1: 14.959 min; 360 Q.344

Method 1: 13.527 min; 418 Q.345

Method 1: 12.808 min; 404 Q.346

Method 1: 13.160 min; 404 Q.347

Method 1: 11.431 min; 312 Q.348

Method 1: 11.698 min; 326 Q.349

Method 1: 12.595 min; 390 Q.350

Method 1: 11.248 min; 312 Q.351

Mp 110-114° C. Q.352

Method 1: 11.715 min; 326 Q.353

Method 1: 12.754 min; 404 Q.354

Method 1: 11.787 min; 326 Q.355

Method 1: 12.370 min; 340 Q.356

Method 1: 12.096 min; 354 Q.357

Method 1: 12.656 min; 368 Q.358

Method 1: 11.887 min; 326 Q.359

Method 1: 12.700 min; 340 Q.360

Method 1: 12.328 min; 340 Q.361

Method 1: 12.882 min; 354 Q.362

Method 1: 15.320 min; 354 Q.363

Method 1: 12.506 min; 341 Q.364

Method 1: 12.385 min; 390 Q.365

Method 1: 13.743 min; 466 Q.366

Method 1: 10.775 min; 328 Q.367

Method 1: 10.377 min; 314 Q.368

Method 1: 11.191 min; 312 Q.369

Mp 120-121° C. Q.370

Method 1: 11.282 min; 423 Q.371

Method 1: 11.875 min; 272 Q.372

Method 1: 10.334 min; 344 Q.373

Method 1: 10.676 min; 358 Q.374

Method 1: 11.096 min; 372 Q.375

Method 1: 11.418 min; 390 Q.376

Method 1: 11.717 min; 413 Q.377

Method 1: 10.791 min; 358 Q.378

Method 1: 12.258 min; 452 Q.379

Mp 168-170° C. Q.380

Method 1: 12.229 min; 304; Trans Q.381

Method 1: 12.388 min; 305; Cis Q.382

Method 1: 12.998 min; 368 Q.383

Method 6: 0.61 min; 336 Q.384

Method 6: 0.67 min; 332 Q.385

Method 3: 1.34 min; 338 Q.386

Method 3: 1.34 min; 424 Q.387

Method 6: 0.55 min; 286 Q.388

Method 6: 0.73 min; 314 Q.389

Method 6: 0.79 min; 328 Q.390

Method 6: 0.79 min; 328 Q.391

Method 6: 0.83 min; 342 Q.392

Method 6: 0.88 min; 356 Q.393

Method 6: 0.69 min; 312 Q.394

Method 6: 0.76 min; 326 Q.395

Method 6: 0.79 min; 420 Q.396

Method 6: 0.60 min; 350 Q.397

Method 6: 0.93 min; 442 Q.398

Method 6: 0.86 min; 392 Q.399

Method 6: 0.89 min; 390 Q.400

Method 6: 0.83 min; 404 Q.401

Method 6: 0.89 min; 404 Q.402

Method 6: 0.88 min; 406 Q.403

Method 6: 0.99 min; 369 Q.404

Method 6: 0.92 min; 406 Q.405

Method 6: 0.54 min; 334 Q.406

Method 1: 8.584 min; 396 Q.407

Method 1: 12.363 min; 392 Q.408

Method 1: 12.632 min; 319; Trans Q.409

Method 1: 12.533 min; 319; Cis Q.410

Method 1: 11.796 min; 304 Q.411

Method 1: 12.661 min; 318 Q.412

Method 1: 14.132 min; 348 Q.413

Method 1: 14.531 min; 362 Q.414

Method 1: 12.019 min; 304 Q.415

Mp 81-83° C. Q.416

Method 1: 14.621 min; 410 Q.417

Method 1: 15.162 min; 404 Q.418

Method 1: 14.413 min; 340 Q.419

Method 1: 13.860 min; 326 Q.420

Method 1: 13.191 min; 418 Q.421

Method 1: 12.542 min; 354 Q.422

Mp 61-63° C. Q.423

Method 1: 12.785 min; 340 Q.424

Method 1: 12.041 min; 326 Q.425

Method 1: 13.378 min; 418 Q.426

Method 1: 13.958 min; 432 Q.427

Method 1: 8.845 min; 374 Q.428

Method 1: 13.142 min; 370 Q.429

Method 1: 10.416 min; 358 Q.430

Mp 122-124° C. Q.431

Method 1: 10.943 min; 310 Q.432

Method 1: 11.341 min; 324 Q.433

Method 1: 12.746 min; 356 Q.434

Method 1: 10.964 min; 278 Q.435

Method 1: 10.497 min; 264 Q.436

Method 1: 12.277 min; 390 Q.437

Method 1: 12.606 min; 368 Q.438

Method 1: 9.727 min; 370 Q.439

Method 1: 12.860 min; 404 Q.440

Method 1: 10.054 min; 262 Q.441

Method 1: 12.781 min; 276 Q.442

Method 1: 13.922 min; 326 Q.443

Method 1: 12.141 min; 342 Q.444

Method 1: 12.715 min; 356 Q.445

Method 1: 11.909 min; 412 Q.446

Method 1: 9.174 min; 356 Q.447

Method 1: 9.174 min; 356 Q.448

Mp 106-107° C. Q.449

Method 1: 12.070 min; 354 Q.450

Method 1: 12.652 min; 368 Q.451

Method 1: 10.212 min; 385 Q.452

Method 1: 11.435 min; 324 Q.453

Method 1: 11.704 min; 338 Q.454

Mp 85-87° C.

Biological Examples Blumeria graminis f. sp. tritici (Erysiphe graminisf. sp. tritici)/Wheat/Leaf Disc Preventative (Powdery Mildew on Wheat)

Wheat leaf segments cv. Kanzler were placed on agar in a multiwell plate(24-well format) and sprayed with the formulated test compound dilutedin water. The leaf disks were inoculated by shaking powdery mildewinfected plants above the test plates 1 day after application. Theinoculated leaf disks were incubated at 20° C. and 60% rh under a lightregime of 24 h darkness followed by 12 h light/12 h darkness in aclimate chamber and the activity of a compound was assessed as percentdisease control compared to untreated when an appropriate level ofdisease damage appears on untreated check leaf segments (6-8 days afterapplication).

The following compounds gave at 200 ppm give at least 50% diseasecontrol in this test when compared to untreated control leaf disks underthe same conditions, which show extensive disease development:

Q.001, Q.004, Q.005, Q.006, Q.007, Q.010, Q.011, Q.012, Q.013, Q.014,Q.015, Q.016, Q.017, Q.018, Q.019, Q.020, Q.021, Q.022, Q.023, Q.024,Q.025, Q.026, Q.027, Q.028, Q.029, Q.030, Q.031, Q.032, Q.033, Q.034,Q.035, Q.036, Q.037, Q.038, Q.039, Q.040, Q.041, Q.042, Q.043, Q.044,Q.045, Q.046, Q.047, Q.048, Q.049, Q.050, Q.051, Q.052, Q.053, Q.054,Q.055, Q.057, Q.058, Q.059, Q.060, Q.062, Q.063, Q.064, Q.065, Q.066,Q.067, Q.068, Q.069, Q.070, Q.071, Q.072, Q.073, Q.074, Q.075, Q.076,Q.077, Q.078, Q.079, Q.080, Q.081, Q.082, Q.084, Q.085, Q.086, Q.087,Q.088, Q.089, Q.090, Q.091, Q.092, Q.093, Q.094, Q.095, Q.097, Q.098,Q.099, Q.100, Q.101, Q.102, Q.103, Q.104, Q.105, Q.106, Q.108, Q.109,Q.110, Q.111, Q.112, Q.113, Q.114, Q.115, Q.116, Q.117, Q.118, Q.119,Q.120, Q.121, Q.122, Q.123, Q.124, Q.125, Q.126, Q.127, Q.128, Q.129,Q.130, Q.131, Q.132, Q.133, Q.134, Q.135, Q.136, Q.140, Q.141, Q.142,Q.143, Q.144, Q.145, Q.146, Q.147, Q.148, Q.149, Q.151, Q.152, Q.153,Q.154, Q.155, Q.156, Q.158, Q.160, Q.161, Q.162, Q.163, Q.164, Q.165,Q.166, Q.167, Q.168, Q.170, Q.171, Q.172, Q.174, Q.175, Q.176, Q.177,Q.178, Q.179, Q.180, Q.181, Q.183, Q.184, Q.185, Q.186, Q.187, Q.188,Q.191, Q.192, Q.193, Q.195, Q.196, Q.197, Q.198, Q.199, Q.200, Q.201,Q.202, Q.203, Q.204, Q.205, Q.206, Q.207, Q.208, Q.209, Q.211, Q.212,Q.213, Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221, Q.222,Q.223, Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.230, Q.231, Q.233,Q.235, Q.238, Q.239, Q.240, Q.241, Q.242, Q.243, Q.244, Q.245, Q.246,Q.247, Q.248, Q.249, Q.250, Q.251, Q.255, Q.256, Q.260, Q.261, Q.262,Q.263, Q.265, Q.267, Q.269, Q.270, Q.271, Q.272, Q.273, Q.274, Q.275,Q.276, Q.277, Q.278, Q.280, Q.281, Q.282, Q.283, Q.284, Q.285, Q.286,Q.287, Q.288, Q.289, Q.290, Q.291, Q.292, Q.293, Q.294, Q.296, Q.297,Q.298, Q.299, Q.300, Q.301, Q.302, Q.303, Q.304, Q.305, Q.306, Q.307,Q.308, Q.309, Q.310, Q.312, Q.315, Q.316, Q.317, Q.318, Q.319, Q.320,Q.321, Q.322, Q.323, Q.324, Q.325, Q.326, Q.327, Q.329, Q.330, Q.331,Q.332, Q.333, Q.334, Q.335, Q.336, Q.337, Q.338, Q.339, Q.340, Q.341,Q.342, Q.343, Q.344, Q.345, Q.346, Q.347, Q.349, Q.350, Q.351, Q.352,Q.353, Q.354, Q.355, Q.356, Q.357, Q.358, Q.359, Q.360, Q.361, Q.364,Q.365, Q.367, Q.368, Q.369, Q.370, Q.371, Q.373, Q.374, Q.375, Q.376,Q.378, Q.380, Q.381, Q.382, Q.383, Q.384, Q.385, Q.386, Q.388, Q.389,Q.390, Q.391, Q.392, Q.393, Q.394, Q.397, Q.398, Q.400, Q.401

Puccinia recondita f. sp. tritici/Wheat/Leaf Disc Preventative (BrownRust)

Wheat leaf segments cv. Kanzler were placed on agar in multiwell plates(24-well format) and sprayed with the formulated test compound dilutedin water. The leaf disks were inoculated with a spore suspension of thefungus 1 day after application. The inoculated leaf segments wereincubated at 19° C. and 75% rh under a light regime of 12 h light/12 hdarkness in a climate cabinet and the activity of a compound wasassessed as percent disease control compared to untreated when anappropriate level of disease damage appears in untreated check leafsegments (7-9 days after application).

The following compounds gave at 200 ppm gave at least 50% diseasecontrol in this test when compared to untreated control leaf disks underthe same conditions, which show extensive disease development:

Q.001, Q.002, Q.003, Q.004, Q.005, Q.006, Q.007, Q.008, Q.009, Q.010,Q.011, Q.012, Q.013, Q.014, Q.015, Q.016, Q.017, Q.018, Q.019, Q.020,Q.021, Q.022, Q.023, Q.024, Q.025, Q.026, Q.027, Q.028, Q.029, Q.030,Q.031, Q.032, Q.033, Q.034, Q.035, Q.036, Q.037, Q.038, Q.039, Q.040,Q.041, Q.042, Q.043, Q.044, Q.045, Q.046, Q.047, Q.048, Q.049, Q.050,Q.051, Q.052, Q.053, Q.054, Q.055, Q.056, Q.057, Q.058, Q.059, Q.060,Q.061, Q.062, Q.063, Q.064, Q.065, Q.066, Q.067, Q.068, Q.069, Q.070,Q.071, Q.072, Q.073, Q.074, Q.075, Q.076, Q.077, Q.078, Q.079, Q.080,Q.081, Q.082, Q.083, Q.084, Q.085, Q.086, Q.087, Q.088, Q.089, Q.090,Q.091, Q.092, Q.093, Q.094, Q.095, Q.096, Q.097, Q.098, Q.099, Q.100,Q.101, Q.102, Q.103, Q.104, Q.105, Q.106, Q.107, Q.108, Q.109, Q.110,Q.111, Q.112, Q.113, Q.114, Q.115, Q.116, Q.117, Q.118, Q.119, Q.120,Q.121, Q.122, Q.123, Q.124, Q.125, Q.126, Q.127, Q.128, Q.129, Q.130,Q.131, Q.132, Q.133, Q.134, Q.135, Q.136, Q.137, Q.138, Q.140, Q.141,Q.142, Q.143, Q.144, Q.145, Q.146, Q.147, Q.148, Q.149, Q.150, Q.151,Q.152, Q.153, Q.154, Q.155, Q.156, Q.157, Q.158, Q.159, Q.160, Q.161,Q.162, Q.163, Q.164, Q.165, Q.166, Q.167, Q.168, Q.169, Q.170, Q.171,Q.172, Q.173, Q.174, Q.175, Q.176, Q.177, Q.178, Q.179, Q.180, Q.181,Q.182, Q.183, Q.184, Q.185, Q.186, Q.187, Q.188, Q.189, Q.190, Q.191,Q.192, Q.193, Q.194, Q.195, Q.196, Q.197, Q.198, Q.199, Q.200, Q.201,Q.202, Q.203, Q.204, Q.205, Q.206, Q.207, Q.208, Q.209, Q.210, Q.211,Q.212, Q.213, Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221,Q.222, Q.223, Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.230, Q.231,Q.232, Q.233, Q.234, Q.235, Q.236, Q.237, Q.238, Q.239, Q.240, Q.241,Q.242, Q.243, Q.244, Q.245, Q.246, Q.247, Q.248, Q.249, Q.250, Q.251,Q.252, Q.253, Q.254, Q.255, Q.256, Q.257, Q.258, Q.259, Q.260, Q.261,Q.262, Q.263, Q.264, Q.265, Q.266, Q.267, Q.268, Q.269, Q.270, Q.271,Q.272, Q.273, Q.274, Q.275, Q.276, Q.277, Q.278, Q.279, Q.280, Q.281,Q.282, Q.283, Q.284, Q.285, Q.286, Q.287, Q.288, Q.289, Q.290, Q.291,Q.292, Q.293, Q.294, Q.295, Q.296, Q.297, Q.298, Q.299, Q.300, Q.301,Q.302, Q.303, Q.304, Q.305, Q.306, Q.307, Q.308, Q.309, Q.310, Q.311,Q.312, Q.313, Q.314, Q.315, Q.316, Q.317, Q.318, Q.319, Q.320, Q.321,Q.322, Q.323, Q.324, Q.325, Q.326, Q.327, Q.328, Q.329, Q.330, Q.331,Q.332, Q.333, Q.334, Q.335, Q.336, Q.337, Q.338, Q.339, Q.340, Q.341,Q.342, Q.343, Q.344, Q.345, Q.346, Q.347, Q.348, Q.349, Q.350, Q.351,Q.352, Q.353, Q.354, Q.355, Q.356, Q.357, Q.358, Q.359, Q.360, Q.361,Q.362, Q.363, Q.364, Q.365, Q.366, Q.367, Q.368, Q.369, Q.370, Q.371,Q.372, Q.373, Q.374, Q.375, Q.376, Q.377, Q.378, Q.379, Q.380, Q.381,Q.382, Q.383, Q.384, Q.385, Q.386, Q.387, Q.388, Q.389, Q.390, Q.391,Q.392, Q.393, Q.394, Q.397, Q.398, Q.400, Q.401

Puccinia recondita f. sp. tritici/Wheat/Leaf Disc Curative (Brown Rust)

Wheat leaf segments cv. Kanzler are placed on agar in multiwell plates(24-well format). The leaf segments are inoculated with a sporesuspension of the fungus. Plates were stored in darkness at 19° C. and75% rh. The formulated test compound diluted in water was applied 1 dayafter inoculation. The leaf segments were incubated at 19° C. and 75% rhunder a light regime of 12 h light/12 h darkness in a climate cabinetand the activity of a compound was assessed as percent disease controlcompared to untreated when an appropriate level of disease damageappears in untreated check leaf segments (6-8 days after application).

The following compounds gave at 200 ppm gaive at least 50% diseasecontrol in this test when compared to untreated control leaf disks underthe same conditions, which show extensive disease development:

Q.001, Q.004, Q.005, Q.006, Q.007, Q.010, Q.011, Q.012, Q.013, Q.014,Q.015, Q.016, Q.018, Q.019, Q.020, Q.021, Q.022, Q.023, Q.024, Q.025,Q.026, Q.027, Q.028, Q.029, Q.030, Q.031, Q.032, Q.033, Q.034, Q.035,Q.036, Q.037, Q.038, Q.039, Q.040, Q.041, Q.042, Q.043, Q.044, Q.045,Q.046, Q.047, Q.048, Q.049, Q.050, Q.051, Q.052, Q.053, Q.054, Q.055,Q.057, Q.058, Q.059, Q.060, Q.062, Q.063, Q.064, Q.065, Q.066, Q.067,Q.068, Q.069, Q.070, Q.071, Q.072, Q.073, Q.074, Q.075, Q.076, Q.077,Q.078, Q.079, Q.080, Q.081, Q.082, Q.084, Q.085, Q.086, Q.087, Q.088,Q.089, Q.090, Q.091, Q.092, Q.093, Q.094, Q.095, Q.096, Q.097, Q.098,Q.099, Q.100, Q.101, Q.102, Q.103, Q.104, Q.105, Q.106, Q.109, Q.110,Q.111, Q.112, Q.113, Q.114, Q.115, Q.116, Q.117, Q.118, Q.119, Q.120,Q.121, Q.122, Q.123, Q.124, Q.126, Q.127, Q.128, Q.129, Q.130, Q.131,Q.132, Q.133, Q.134, Q.135, Q.136, Q.140, Q.141, Q.143, Q.144, Q.145,Q.146, Q.147, Q.148, Q.149, Q.151, Q.152, Q.153, Q.154, Q.155, Q.156,Q.158, Q.159, Q.160, Q.161, Q.162, Q.163, Q.164, Q.165, Q.166, Q.167,Q.168, Q.169, Q.170, Q.171, Q.172, Q.174, Q.175, Q.176, Q.177, Q.178,Q.179, Q.180, Q.181, Q.182, Q.183, Q.184, Q.185, Q.186, Q.188, Q.191,Q.192, Q.193, Q.194, Q.195, Q.196, Q.197, Q.198, Q.199, Q.200, Q.201,Q.203, Q.204, Q.205, Q.206, Q.207, Q.208, Q.209, Q.211, Q.212, Q.213,Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221, Q.222, Q.223,Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.230, Q.231, Q.232, Q.233,Q.235, Q.236, Q.238, Q.239, Q.240, Q.241, Q.242, Q.243, Q.244, Q.246,Q.247, Q.248, Q.249, Q.250, Q.251, Q.253, Q.254, Q.255, Q.256, Q.257,Q.258, Q.260, Q.261, Q.262, Q.263, Q.265, Q.269, Q.270, Q.271, Q.273,Q.274, Q.275, Q.276, Q.277, Q.278, Q.279, Q.280, Q.281, Q.282, Q.283,Q.284, Q.285, Q.286, Q.287, Q.288, Q.289, Q.290, Q.291, Q.292, Q.293,Q.294, Q.296, Q.297, Q.298, Q.299, Q.300, Q.301, Q.302, Q.303, Q.304,Q.305, Q.306, Q.307, Q.308, Q.309, Q.310, Q.311, Q.315, Q.316, Q.317,Q.318, Q.319, Q.320, Q.321, Q.322, Q.323, Q.324, Q.325, Q.326, Q.327,Q.329, Q.330, Q.331, Q.332, Q.333, Q.334, Q.335, Q.336, Q.337, Q.338,Q.339, Q.340, Q.341, Q.342, Q.344, Q.345, Q.346, Q.347, Q.348, Q.349,Q.350, Q.351, Q.352, Q.353, Q.354, Q.355, Q.356, Q.357, Q.358, Q.359,Q.360, Q.361, Q.362, Q.363, Q.364, Q.365, Q.366, Q.367, Q.368, Q.369,Q.370, Q.371, Q.372, Q.373, Q.374, Q.375, Q.376, Q.377, Q.378, Q.380,Q.381, Q.382, Q.383, Q.384, Q.385, Q.386, Q.388, Q.389, Q.390, Q.391,Q.392, Q.393, Q.394, Q.397, Q.398, Q.400, Q.401

Pyrenophora teres/Barley/Leaf Disc Preventative (Net Blotch)

Barley leaf segments cv. Hasso were placed on agar in a multiwell plate(24-well format) and sprayed with the formulated test compound dilutedin water. The leaf segments were inoculated with a spore suspension ofthe fungus 2 days after application. The inoculated leaf segments wereincubated at 20° C. and 65% rh under a light regime of 12 h light/12 hdarkness in a climate cabinet and the activity of a compound wasassessed as disease control compared to untreated when an appropriatelevel of disease damage appears in untreated check leaf segments (5-7days after application).

The following compounds gave at 200 ppm give at least 50% diseasecontrol in this test when compared to untreated control leaf disks underthe same conditions, which show extensive disease development:

Q.001, Q.004, Q.005, Q.007, Q.011, Q.012, Q.013, Q.014, Q.015, Q.016,Q.018, Q.019, Q.020, Q.021, Q.022, Q.023, Q.024, Q.025, Q.026, Q.027,Q.028, Q.029, Q.032, Q.033, Q.034, Q.035, Q.038, Q.039, Q.041, Q.042,Q.043, Q.044, Q.046, Q.047, Q.052, Q.053, Q.054, Q.055, Q.057, Q.059,Q.062, Q.063, Q.066, Q.067, Q.069, Q.070, Q.071, Q.074, Q.075, Q.076,Q.079, Q.082, Q.086, Q.087, Q.088, Q.089, Q.090, Q.091, Q.093, Q.095,Q.097, Q.099, Q.100, Q.101, Q.102, Q.103, Q.105, Q.106, Q.110, Q.111,Q.113, Q.115, Q.116, Q.117, Q.118, Q.119, Q.120, Q.121, Q.122, Q.124,Q.125, Q.127, Q.128, Q.129, Q.131, Q.133, Q.136, Q.141, Q.143, Q.144,Q.146, Q.148, Q.153, Q.154, Q.155, Q.158, Q.160, Q.161, Q.162, Q.163,Q.164, Q.166, Q.167, Q.168, Q.169, Q.170, Q.174, Q.175, Q.176, Q.178,Q.180, Q.183, Q.184, Q.186, Q.191, Q.193, Q.195, Q.196, Q.197, Q.198,Q.199, Q.200, Q.201, Q.202, Q.203, Q.204, Q.206, Q.207, Q.208, Q.209,Q.211, Q.212, Q.214, Q.215, Q.216, Q.217, Q.218, Q.219, Q.220, Q.221,Q.222, Q.223, Q.224, Q.225, Q.226, Q.227, Q.228, Q.229, Q.231, Q.232,Q.233, Q.235, Q.236, Q.237, Q.238, Q.240, Q.241, Q.242, Q.243, Q.244,Q.245, Q.246, Q.247, Q.248, Q.249, Q.250, Q.251, Q.252, Q.253, Q.255,Q.256, Q.260, Q.261, Q.262, Q.269, Q.275, Q.277, Q.278, Q.280, Q.282,Q.284, Q.285, Q.286, Q.289, Q.291, Q.292, Q.293, Q.298, Q.299, Q.301,Q.302, Q.304, Q.308, Q.311, Q.315, Q.316, Q.320, Q.322, Q.324, Q.326,Q.329, Q.334, Q.335, Q.336, Q.337, Q.340, Q.344, Q.346, Q.349, Q.352,Q.353, Q.354, Q.355, Q.357, Q.358, Q.361, Q.363, Q.364, Q.366, Q.370,Q.371, Q.375, Q.376, Q.377, Q.378, Q.380, Q.382, Q.386, Q.389, Q.390,Q.391, Q.392, Q.393, Q.394, Q.398, Q.400

In the following Tables ‘Activity (%)’ means the assessed experimentalactivity (% disease control in this test when compared to untreatedcontrol leaf disks under the same conditions, which show extensivedisease development) and “P” is the expected value calculated (expected)activity according to the COLBY formula (see above). The column headed‘S?’ indicates whether or not synergy was observed, with ‘y’ meaningthat synergy was observed.

In the following tables, compound (V) isN-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide,compound (VI) is3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-methyl-2-(2,4,6-trichlorophenyl)ethyl]-1H-pyrazole-4-carboxamide,compound (VII) is[3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluoro-phenyl)-isoxazol-4-yl]-pyridin-3-yl-methanol.

Monographella nivalis (syn. Microdochium nivale, Fusarium nivale), snowmould, foot rot of cereals

Conidia of the fungus from cryogenic storage were directly mixed intonutrient broth (PDB potato dextrose broth). After placing a (DMSO)solution of the test compounds into a microtiter plate (96-well format)the nutrient broth containing the fungal spores was added. The testplates were incubated at 24° C. and activity was determined visuallyafter 72 hrs

Compound Q.135 (V) Activity rate ppm rate ppm (%) P S? 0.0625 20 0.031250 0.015625 0 0.0078125 0 0.0625 50 0.03125 0 0.0625 0.03125 50 20 y0.03125 0.03125 50 0 y 0.03125 0.0625 70 50 y 0.015625 0.03125 20 0 y0.015625 0.0625 70 50 y 0.0078125 0.03125 70 0 y Q.135 MetconazoleActivity rate ppm rate ppm (%) P S? 0.0625 70 0.03125 0 0.25 0 0.125 00.0625 0 0.03125 0 0.015625 0 0.0625 0.25 100 70 y 0.0625 0.125 100 70 y0.0625 0.0625 100 70 y 0.0625 0.03125 100 70 y 0.0625 0.015625 100 70 y0.03125 0.125 100 0 y 0.03125 0.0625 70 0 y 0.03125 0.03125 50 0 y0.03125 0.015625 20 0 y cis- Q.135 Jasmone Activity rate ppm rate ppm(%) P S? 0.0625 50 0.03125 0 1.25 0 0.625 0 0.3125 0 0.15625 0 0.06251.25 100 50 y 0.0625 0.625 90 50 y 0.0625 0.3125 100 50 y 0.0625 0.15625100 50 y 0.03125 1.25 100 0 y 0.03125 0.625 50 0 y 0.03125 0.3125 20 0 yQ.135 2,4-D Activity rate ppm rate ppm (%) P S? 0.625 50 0.3125 0 2.5 01.25 0 0.625 0 0.3125 0 0.625 2.5 100 50 y 0.625 1.25 90 50 y 0.6250.625 90 50 y 0.625 0.3125 90 50 y 0.625 0.15625 100 50 y 0.3125 1.25 200 y Q.135 Azoxystrobin Activity rate ppm rate ppm (%) P S? 0.125 700.0625 0 0.00625 70 0.003125 20 0.0015625 0 0.125 0.003125 90 70 y0.0625 0.00625 100 70 y 0.0625 0.0015625 20 0 y Q.135 FenpropimorphActivity rate ppm rate ppm (%) P S? 0.03125 20 0.125 0 0.0625 0 0.031250 0.015625 0 0.0078125 0 0.03125 0.125 100 20 y 0.03125 0.0625 90 20 y0.03125 0.03125 90 20 y 0.03125 0.015625 70 20 y 0.03125 0.0078125 90 20y Q.135 Bicyclopyrone Activity rate ppm rate ppm (%) P S? 0.0625 200.03125 0 0.3125 0 0.15625 0 0.078125 0 0.0625 0.15625 90 20 y 0.031250.078125 20 0 y 0.0625 0.3125 70 20 y Q.135 Abamectin Activity rate ppmrate ppm (%) P S? 0.0625 20 2.5 0 1.25 0 0.625 0 0.3125 0 0.15625 00.0625 0.15625 70 20 y 0.0625 0.3125 50 20 y 0.0625 0.625 20 20 y 0.06251.25 50 20 y 0.0625 2.5 100 20 y Q.135 Thiamethoxam Activity rate ppmrate ppm (%) P S? 0.125 70 0.0625 20 5 0 2.5 0 0.625 0 0.3125 0 0.1250.3125 100 70 y 0.125 0.625 90 70 y 0.0625 0.3125 50 20 y 0.125 0.25 9070 y 0.125 0.5 100 70 y 0.0625 0.25 70 20 y Q.135 Propiconazole Activityrate ppm rate ppm (%) P S? 0.0625 70 0.03125 0 0.25 0 0.125 0 0.0625 00.03125 0 0.015625 0 0.0625 0.015625 90 70 y 0.0625 0.03125 100 70 y0.0625 0.0625 100 70 y 0.03125 0.015625 50 0 y 0.03125 0.03125 20 0 y0.0625 0.125 100 70 y 0.03125 0.0625 50 0 y 0.0625 0.25 100 70 y 0.031250.125 70 0 y Q.135 Glufosinate Activity rate ppm rate ppm (%) P S?0.0625 70 0.03125 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.0625 0.3125 90 70 y0.0625 0.625 70 70 0.0625 1.25 90 70 y 0.03125 0.625 20 0 y 0.0625 2.590 70 y 0.03125 1.25 20 0 y Q.135 Flutriafol Activity rate ppm rate ppm(%) P S? 0.0625 70 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 0.25 100 70y 0.0625 0.125 90 70 y 0.0625 0.0625 90 70 y 0.0625 0.03125 90 70 yQ.135 Trinexapacethyl Activity rate ppm rate ppm (%) P S? 0.0625 500.03125 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.12625 0 0.0625 2.5 100 50 y0.0625 1.25 90 50 y 0.0625 0.625 70 50 y 0.0625 0.3125 90 50 y 0.06250.15625 90 50 y 0.03125 1.25 20 0 y Q.135 Paclobutrazol Activity rateppm rate ppm (%) P S? 0.0625 70 0.03125 0 0.015625 0 1.25 0 0.625 00.3125 0 0.15625 0 0.0625 1.25 100 70 y 0.0625 0.625 100 70 y 0.06250.3125 100 70 y 0.0625 0.15625 100 70 y 0.03125 1.25 100 0 y 0.031250.625 100 0 y 0.03125 0.3125 50 0 y 0.03125 0.15625 20 0 y 0.0156250.625 20 0 y Q.135 Pyraclostrobin Activity rate ppm rate ppm (%) P S?0.125 70 0.0625 0 0.003125 0 0.0015625 0 0.125 0.003125 90 70 y 0.06250.003125 20 0 y 0.0625 0.0015625 20 0 y Q.135 Mandipropamid Activityrate ppm rate ppm (%) P S? 0.125 70 0.0625 20 0.03125 0 0.0625 0 0.031250 0.125 0.0625 90 70 y 0.125 0.03125 90 70 y 0.0625 0.0625 20 20 0.031250.0625 50 0 y Q.135 Carbendazim Activity rate ppm rate ppm (%) P S?0.125 70 0.0625 20 0.0625 0 0.03125 0 0.015625 0 0.125 0.0625 90 70 y0.0625 0.03125 50 20 y 0.0625 0.015625 50 20 y Copper Q.135 hydroxideActivity rate ppm rate ppm (%) P S? 0.125 70 0.0625 20 5 0 2.5 0 1.25 00.625 0 0.3125 0 0.15625 0 0.125 0.3125 100 70 y 0.125 0.625 100 70 y0.125 1.25 100 70 y 0.0625 0.15625 70 20 y 0.0625 0.3125 70 20 y 0.1252.5 100 70 y 0.125 5 100 70 y Manganese Q.135 oxide Activity rate ppmrate ppm (%) P S? 0.0625 20 2.5 0 1.25 0 0.625 0 0.3125 0 0.15625 00.0625 0.15625 70 20 y 0.0625 0.3125 50 20 y 0.0625 0.625 20 20 0.06251.25 70 20 y 0.0625 2.5 90 20 y Q.135 Mesotrione Activity rate ppm rateppm (%) P S? 0.0625 20 0.03125 0 2.5 0 1.25 0 0.625 0 0.3125 0 0.15625 00.078125 0 0.0625 0.15625 70 20 y 0.0625 0.3125 70 20 y 0.0625 0.625 5020 y 0.03125 0.078125 20 0 y 0.03125 0.15625 20 0 y 0.03125 0.3125 0 0 y0.0625 1.25 70 20 y 0.03125 0.625 20 0 y 0.0625 2.5 90 20 y 0.03125 1.2520 0 y Q.135 Prothioconazole Activity rate ppm rate ppm (%) P S? 0.062570 0.03125 0 0.0125 0 0.00625 0 0.003125 0 0.0015625 0 0.0625 0.0015625100 70 y 0.0625 0.003125 100 70 y 0.0625 0.00625 100 70 y 0.031250.0015625 20 0 y 0.03125 0.003125 20 0 y 0.0625 0.0125 100 70 y 0.031250.00625 100 0 y 0.03125 0.0125 100 0 y Q.113 Flutriafol Activity rateppm rate ppm (%) P S? 2 70 1 20 0.5 20 0.25 0 2 0 1 0 0.5 0 0.25 0 2 2100 70 y 2 1 100 70 y 2 0.5 90 70 y 1 2 90 20 y 1 1 70 20 y 1 0.5 70 20y 1 0.25 50 20 y 0.5 2 50 20 y 0.25 1 20 0 y Q.113 Metconazole Activityrate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 0.125 0 1 20 0.5 0 0.25 00.125 0 1 1 100 60 y 1 0.5 100 50 y 1 0.25 100 50 y 0.5 1 100 36 y 0.50.5 100 20 y 0.5 0.25 90 20 y 0.5 0.125 50 20 y 0.25 1 100 20 y 0.25 0.570 0 y 0.25 0.25 50 0 y 0.25 0.125 20 0 y 0.125 0.5 50 0 y 0.125 0.25 200 y 0.125 0.125 20 0 y Q.113 Penflufen Activity rate ppm rate ppm (%) PS? 1 20 0.5 2 0.25 2 0.125 2 1 20 0.5 0 1 1 50 36 y 0.5 1 50 20 y 0.50.5 20 0 y 0.25 1 50 20 y 0.25 0.5 20 0 y 0.125 0.5 20 0 y Q.113 BixafenActivity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.25 20 0.250.25 50 20 y 0.125 0.25 50 20 y 0.0625 0.25 50 20 y Q.113 FenpropimorphActivity rate ppm rate ppm (%) P S? 0.5 20 0.25 0 1 20 0.5 0 0.25 00.125 0 0.0625 0 0.5 1 700 36 y 0.5 0.5 100 20 y 0.5 0.25 100 20 y 0.50.125 100 20 y 0.25 1 100 20 y 0.25 0.5 90 0 y 0.25 0.25 70 0 y 0.250.125 20 0 y 0.25 0.0625 20 0 y Q.113 Prothioconazole Activity rate ppmrate ppm (%) P S? 0.5 0 0.25 0 0.125 0 0.0125 0 0.5 0.0125 90 0 y 0.250.0125 50 0 y 0.125 0.0125 20 0 y Q.113 Propiconazole Activity rate ppmrate ppm (%) P S? 2 70 1 20 0.5 0 0.25 0 1 20 0.5 0 0.25 0 0.125 0 2 0.5100 70 y 2 1 100 76 y 1 0.25 90 20 y 1 0.5 100 20 y 1 1 100 36 y 0.50.125 20 0 y 0.5 0.25 50 0 y 0.5 0.5 90 0 y 0.25 0.125 20 0 y 0.25 0.2520 0 y 0.5 1 100 20 y 0.25 0.5 50 0 y 0.25 1 90 20 y Q.113 PaclobutrazolActivity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 0.125 0 10 0 5 02.5 0 1.25 0 1 10 100 50 y 1 5 100 50 y 1 2.5 90 50 y 0.5 10 70 20 y 0.55 70 20 y 0.5 2.5 50 20 y 0.5 1.25 50 20 y 0.25 10 50 0 y 0.25 5 50 0 y0.25 2.5 50 0 y 0.25 1.25 20 0 y 0.125 5 20 0 y 0.125 2.5 20 0 y Q.113Azoxystrobin Activity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 00.03125 0 0.00625 50 0.25 0.00625 70 50 y 0.125 0.00625 70 50 y 0.06250.00625 50 50 0.03125 0.00625 100 50 y Q.113 Cyprodinil Activity rateppm rate ppm (%) P S? 0.015625 0 0.0078125 0 0.00390625 0 0.003125 200.0015625 0 0.015625 0.003125 50 20 y 0.0078125 0.0015625 20 0 y0.0078125 0.003125 50 20 y 0.00390625 0.0015625 20 0 y Q.113 AbamectinActivity rate ppm rate ppm (%) P S? 2 70 1 20 0.5 0 20 50 10 0 5 0 2 10100 70 y 1 5 50 20 y 2 20 100 85 y 1 10 50 20 y 1 20 100 60 y 0.5 10 200 y 0.5 20 70 50 y Q.113 Mesotrione Activity rate ppm rate ppm (%) P S?1 20 0.5 0 5 0 2.5 0 1 2.5 50 20 y 1 5 50 20 y 0.5 2.5 20 0 y CompoundQ.062 (V) Activity rate ppm rate ppm (%) P S? 0.0625 0 0.03125 00.015625 0 0.125 70 0.0625 50 0.03125 0 0.0625 0.125 100 70 y 0.031250.0625 70 50 y 0.015625 0.03125 20 0 y 0.03125 0.125 90 70 y 0.0156250.0625 70 50 y Compound Q.062 (VI) Activity rate ppm rate ppm (%) P S?0.03125 0 0.015625 0 0.125 50 0.0625 0 0.03125 0.125 70 50 y 0.031250.0625 20 0 y 0.015625 0.0625 20 0 y Q.062 Chlorothalonil Activity rateppm rate ppm (%) P S? 0.5 50 0.25 20 0.125 0 0.125 70 0.0625 20 0.031250 0.25 0.0625 50 36 y 0.5 0.125 100 85 y 0.125 0.0625 50 20 y 0.1250.03125 20 0 y Q.062 Flutriafol Activity rate ppm rate ppm (%) P S? 0.550 0.25 20 0.125 0 0.5 0 0.25 0 0.125 0 0.0625 0 0.5 0.5 90 50 y 0.50.25 90 50 y 0.5 0.125 90 50 y 0.25 0.5 50 20 y 0.25 0.25 50 20 y 0.250.125 50 20 y 0.25 0.0625 50 20 y 0.125 0.5 20 0 y 0.125 0.25 20 0 y0.125 0.125 20 0 y 0.125 0.0625 20 0 y Q.062 Paclobutrazol Activity rateppm rate ppm (%) P S? 0.5 70 0.25 20 0.125 0 10 0 5 0 2.5 0 1.25 0 0.6250 0.5 10 100 70 y 0.5 5 100 70 y 0.5 2.5 100 70 y 0.5 1.25 100 70 y 0.2510 100 20 y 0.25 5 100 20 y 0.25 2.5 90 20 y 0.25 1.25 70 20 y 0.250.625 70 20 y 0.125 5 70 0 y 0.125 2.5 70 0 y 0.125 1.25 50 0 y 0.1250.625 20 0 y cis- Q.062 Jasmone Activity rate ppm rate ppm (%) P S? 0.2520 0.125 0 5 0 2.5 0 1.25 0 0.625 0 0.25 5 50 20 y 0.25 2.5 50 20 y 0.251.25 50 20 y 0.25 0.625 50 20 y 0.125 5 50 0 y 0.125 2.5 50 0 y 0.1251.25 50 0 y Q.062 Penflufen Activity rate ppm rate ppm (%) P S? 2 20 1 00.5 0 0.25 0 1 20 0.5 0 2 1 50 36 y 1 0.5 20 0 y 0.5 1 50 20 y 0.25 0.520 0 y Q.062 Fenpropimorph Activity rate ppm rate ppm (%) P S? 2 20 1 02 20 1 0 0.5 0 0.25 0 2 2 100 36 y 2 1 90 20 y 2 0.5 70 20 y 1 2 70 20 y1 1 50 0 y 1 0.5 20 0 y 1 0.25 20 0 y Q.062 Abamectin Activity rate ppmrate ppm (%) P S? 1 70 0.5 50 20 50 10 0 5 0 1 5 90 70 y 1 10 100 70 y 120 100 85 y 0.5 10 70 50 y 0.5 20 100 75 y Q.062 Propiconazole Activityrate ppm rate ppm (%) P S? 0.5 50 0.25 20 0.125 0 0.0625 0 1 20 0.5 00.25 0 0.125 0 0.0625 0 0.5 0.125 70 50 y 0.5 0.25 100 50 y 0.5 0.5 10050 y 0.25 0.125 50 20 y 0.25 0.25 70 20 y 0.5 1 100 60 y 0.125 0.0625 200 y 0.125 0.125 20 0 y 0.25 0.5 100 20 y 0.125 0.25 50 0 y 0.0625 0.12520 0 y 0.25 1 100 36 y 0.125 0.5 70 0 y 0.0625 0.25 20 0 y Q.062Metconazole Activity rate ppm rate ppm (%) P S? 0.5 50 0.25 20 0.125 00.0625 0 1 20 0.5 0 0.25 0 0.125 0 0.0625 0 0.5 1 100 60 y 0.5 0.5 10050 y 0.5 0.25 70 50 y 0.5 0.125 100 50 y 0.25 1 100 36 y 0.25 0.5 100 20y 0.25 0.25 90 20 y 0.25 0.125 20 20 0.25 0.0625 50 20 y 0.125 0.5 90 0y 0.125 0.25 50 0 y 0.125 0.125 20 0 y 0.0625 0.25 20 0 y Q.062Trinexapacethyl Activity rate ppm rate ppm (%) P S? 0.5 70 0.25 20 0.1250 5 0 2.5 0 1.25 0 0.625 0 0.5 5 90 70 y 0.5 2.5 90 70 y 0.5 1.25 90 70y 0.25 5 50 20 y 0.25 1.25 50 20 y 0.25 0.625 50 20 y 0.125 5 20 0 y0.125 2.5 20 0 y Q.062 2,4-D Activity rate ppm rate ppm (%) P S? 0.5 700.25 20 0.125 0 10 0 5 0 2.5 0 1.25 0 0.625 0 0.5 10 90 70 y 0.5 5 90 70y 0.5 2.5 90 70 y 0.5 1.25 90 70 y 0.25 10 50 20 y 0.25 5 50 20 y 0.252.5 50 20 y 0.25 1.25 50 20 y 0.25 0.625 50 20 y 0.125 5 20 0 y 0.1252.5 20 0 y 0.125 1.25 20 0 y Q.062 Pyraclostrobin Activity rate ppm rateppm (%) P S? 0.0625 0 0.03125 0 0.015625 0 0.0125 50 0.00625 0 0.06250.0125 70 50 y 0.03125 0.0125 70 50 y 0.03125 0.00625 20 0 y 0.0156250.00625 20 0 y Q.062 Mesotrione Activity rate ppm rate ppm (%) P S? 1 7020 0 10 0 5 0 1 5 90 70 y 1 10 90 70 y 1 20 90 70 y Q.062Prothioconazole Activity rate ppm rate ppm (%) P S? 0.5 50 0.25 20 0.1250 0.0625 0 0.0125 0 0.5 0.0125 100 50 y 0.25 0.0125 100 20 y 0.1250.0125 50 0 y 0.0625 0.0125 20 0 y Q.062 Glufosinate Activity rate ppmrate ppm (%) P S? 0.125 0 5 0 2.5 0 1.25 0 0.125 1.25 20 0 y 0.125 2.520 0 y 0.125 5 20 0 y

Botrytis cinerea (Gray mould)

Conidia of the fungus from cryogenic storage were directly mixed intonutrient broth (PDB potato dextrose broth). After placing a (DMSO)solution of the test compounds into a microtiter plate (96-well format)the nutrient broth containing the fungal spores was added. The testplates were incubated at 24° C. and the activity was determined visuallyafter 72 hrs.

Q.135 Fluxapyroxad Activity rate ppm rate ppm (%) P S? 0.03125 00.015625 0 0.0078125 0 0.00390625 0 0.0625 50 0.03125 20 0.015625 200.0078125 0 0.03125 0.0625 70 50 y 0.015625 0.03125 50 20 y 0.00781250.015625 50 20 y 0.00390625 0.0078125 20 0 y 0.015625 0.0625 70 50 y0.0078125 0.03125 50 20 y 0.00390625 0.015625 50 20 y Compound Q.135 (V)Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 00.125 70 0.0625 70 0.03125 50 0.015625 20 0.015625 0.03125 70 50 y0.0078125 0.015625 50 20 y 0.03125 0.125 90 70 y 0.015625 0.0625 70 700.0078125 0.03125 70 50 y Q.135 Flutriafol Activity rate ppm rate ppm(%) P S? 1 50 0.5 20 0.25 0 0.125 0 1 0 0.5 0 0.25 0 0.125 0 1 1 100 50y 1 0.5 100 50 y 1 0.25 100 50 y 0.5 1 90 20 y 0.5 0.5 90 20 y 0.5 0.2590 20 y 0.5 0.125 70 20 y 0.25 1 70 0 y 0.25 0.5 50 0 y 0.25 0.25 50 0 y0.25 0.125 50 0 y 0.125 0.5 20 0 y Q.135 Metconazole Activity rate ppmrate ppm (%) P S? 0.125 0 0.0625 0 0.03125 0 0.03125 0 0.015625 0 0.1250.03125 70 0 y 0.0625 0.03125 50 0 y 0.0625 0.015625 20 0 y 0.031250.03125 50 0 y cis- Q.135 Jasmone Activity rate ppm rate ppm (%) P S? 150 0.5 20 0.25 0 5 0 2.5 0 1.25 0 0.625 0 1 5 90 50 y 1 2.5 90 50 y 0.52.5 50 20 y 0.5 1.25 50 20 y 0.25 1.25 20 0 y 0.25 0.625 20 0 y Q.1352,4-D Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 10 0 5 0 2.5 0 110 90 50 y 1 5 100 50 y 1 2.5 90 50 y 0.5 10 50 20 y 0.5 5 50 20 y 0.52.5 50 20 y 0.5 1.25 50 20 y Q.135 Pyraclostrobin Activity rate ppm rateppm (%) P S? 1 20 0.5 0 0.25 0 0.2 20 0.1 0 0.05 0 0.025 0 1 0.2 70 36 y1 0.1 50 20 y 1 0.05 50 20 y 1 0.025 50 20 y 0.5 0.2 50 20 y 0.5 0.1 500 y 0.5 0.05 20 0 y 0.5 0.025 20 0 y 0.25 0.1 20 0 y 0.25 0.05 20 0 yQ.135 Picoxystrobin Activity rate ppm rate ppm (%) P S? 1 20 0.5 0 0.250 0.125 0 2 50 1 50 0.5 50 0.25 50 1 2 90 60 y 1 1 90 60 y 1 0.5 90 60 y0.5 2 90 50 y 0.5 1 70 50 y 0.5 0.5 70 50 y 0.5 0.25 70 50 y 0.25 1 7050 y 0.25 0.58 70 50 y 0.25 0.25 70 50 y 0.125 0.5 70 50 y 0.125 0.25 7050 y Q.135 Fenpropimorph Activity rate ppm rate ppm (%) P S? 1 50 0.5 200.25 0 0.125 0 0.0625 0 0.25 0 0.125 0 0.0625 0 1 0.25 100 50 y 0.5 0.25100 20 y 0.5 0.125 100 20 y 0.25 0.25 100 0 y 0.25 0.125 100 0 y 0.250.0625 90 0 y 0.125 0.25 100 0 y 0.125 0.125 100 0 y 0.125 0.0625 70 0 y0.0625 0.25 90 0 y 0.0625 0.125 70 0 y 0.0625 0.0625 20 0 y Q.135Bicyclopyrone Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 5 0 2.5 01.25 0 1 2.5 70 50 y 1 5 70 50 y 0.5 1.25 50 20 y 0.5 2.5 50 20 y Q.135Thiamethoxam Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 2.50 1.25 0 0.625 0 1 2.5 70 50 y 0.5 1.25 50 20 y 0.25 0.625 20 0 y Q.135Mesotrione Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 0 10 0 50 2.5 0 1.25 0 0.625 0 1 2.5 70 50 y 1 5 70 50 y 0.5 1.25 50 20 y 0.52.5 50 20 y 0.25 0.625 20 0 y 0.25 1.25 20 0 y 0.5 10 50 20 y Q.135Propiconazole Activity rate ppm rate ppm (%) P S? 2 70 1 50 0.5 20 0.250 0.125 0 0.5 50 0.25 0 0.125 0 0.0625 0 2 0.5 100 85 y 1 0.25 100 20 y1 0.5 100 60 y 0.5 0.125 70 20 y 0.5 0.25 90 20 y 0.5 0.5 100 60 y 0.250.0625 50 0 y 0.25 0.125 70 0 y 0.25 0.25 70 0 y 0.125 0.0625 20 0 y0.125 0.125 20 0 y 0.25 0.5 90 50 y 0.125 0.25 50 0 y 0.125 0.5 70 50 yQ.135 Mandipropamid Activity rate ppm rate ppm (%) P S? 2 70 1 20 0.5 020 0 10 0 5 0 2 10 90 70 y 2 20 90 70 y 1 5 50 20 y 1 10 50 20 y 0.5 520 0 y 1 20 50 20 y 0.5 10 20 0 y 0.5 20 20 0 y Q.135 ChlorotalonilActivity rate ppm rate ppm (%) P S? 0.5 20 0.25 0 0.125 0 0.0625 0 0.2520 0.125 0 0.0625 0 0.5 0.25 90 36 y 0.5 0.125 50 20 y 0.25 0.25 90 20 y0.25 0.125 50 0 y 0.25 0.0625 20 0 y 0.125 0.25 50 20 y 0.125 0.125 50 0y 0.125 0.0625 20 0 y 0.0625 0.25 50 20 y 0.0625 0.125 20 0 y 0.06250.0625 20 0 y Q.135 Trinexapacethyl Activity rate ppm rate ppm (%) P S?1 50 0.5 20 0.25 0 20 0 10 0 5 0 2.5 0 1.25 0 1 20 90 50 y 1 10 90 50 y1 5 90 50 y 1 2.5 90 50 y 0.5 20 70 20 y 0.5 10 50 20 y 0 5 50 20 y 0.52.5 50 20 y 0.5 1.25 50 20 y 0.25 10 20 0 y 0.25 5 20 0 y 0.25 1.25 20 0y Q.135 Paclobutrazol Activity rate ppm rate ppm (%) P S? 0.5 20 0.25 00.125 0 0.0625 0 2.5 0 1.25 0 0.625 0 0.5 2.5 100 20 y 0.5 1.25 100 20 y0.25 2.5 100 0 y 0.25 1.25 90 0 y 0.25 0.625 70 0 y 0.125 2.5 100 0 y0.125 1.25 70 0 y 0.125 0.625 50 0 y 0.0625 2.5 100 0 y 0.0625 1.25 50 0y Q.135 Azoxystrobin Activity rate ppm rate ppm (%) P S? 2 50 1 20 0.5 00.25 0 0.2 20 0.1 0 0.05 0 0.025 0 2 0.1 90 50 y 2 0.05 70 50 y 1 0.2 7036 y 1 0.1 50 20 y 1 0.05 50 20 y 1 0.025 50 20 y 0.5 0.2 50 20 y 0.50.1 50 0 y 0.5 0.05 20 0 y 0.5 0.025 20 0 y 0.25 0.1 50 0 y 0.25 0.05 200 y 0.25 0.025 20 0 y Q.135 Trifloxystrobin Activity rate ppm rate ppm(%) P S? 0.5 20 0.25 0 0.1 50 0.05 50 0.025 20 0.0125 0 0.5 0.025 50 36y 0.5 0.0125 50 20 y 0.25 0.1 70 50 y 0.25 0.05 50 50 0.25 0.025 50 20 y0.25 0.0125 20 0 y Q.135 Fludioxonil Activity rate ppm rate ppm (%) P S?0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 70 0.03125 0 0.25 0.0625 100 70y 0.125 0.0625 100 70 y 0.125 0.03125 50 0 y 0.0625 0.0625 100 70 y0.0625 0.03125 50 0 y 0.03125 0.0625 100 70 y 0.03125 0.03125 50 0 yCopper Q.135 hydroxide Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 50 2.5 0 1.25 0 1 2.5 70 50 y 1 5 70 50 y 0.5 1.25 50 20 y 0.5 2.5 50 20y Q.135 Abamectin Activity rate ppm rate ppm (%) P S? 1 50 0.5 20 0.25 020 0 10 0 5 0 2.5 0 1.25 0 1 2.5 90 50 y 1 5 90 50 y 1 10 70 50 y 0.51.25 50 20 y 0.5 2.5 70 20 y 0.5 5 50 20 y 1 20 70 50 y 0.25 1.25 20 0 y0.25 2.5 20 0 y 0.5 10 50 20 y 0.25 5 50 0 y 0.5 20 50 20 y 0.25 10 50 0y Q.135 Prothioconazole Activity rate ppm rate ppm (%) P S? 0.5 20 0.250 0.125 0 0.05 50 0.025 0 0.0125 0 0.00625 0 2 0.05 100 85 y 1 0.025 10020 y 1 0.05 100 60 y 0.5 0.0125 90 20 y 0.5 0.025 100 20 y 0.5 0.05 10060 y 0.25 0.00625 50 0 y 0.25 0.0125 70 0 y 0.25 0.025 90 0 y 0.1250.00625 20 0 y 0.125 0.0125 50 0 y 0.125 0.05 100 50 y 0.125 0.025 70 0y 0.125 0.05 100 50 y Q.135 Glufosinate Activity rate ppm rate ppm (%) PS? 1 20 0.5 0 0.25 0 20 0 10 0 5 0 2.5 0 1 2.5 50 20 y 1 5 50 20 y 0.52.5 20 0 y 1 20 50 20 y 0.5 10 20 0 y 0.5 20 20 0 y 0.5 10 20 0 y Q.135Procymidone Activity rate ppm rate ppm (%) P S? 1 20 0.5 0 0.25 0 2.5 501.25 0 1 2.5 100 60 y 0.5 1.25 50 0 y 0.25 2.5 90 50 y Q.113Fluxapyroxad Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 00.0078125 0 0.00390625 0 0.0625 50 0.03125 50 0.015625 20 0.0078125 200.03125 0.0625 70 50 y 0.015625 0.03125 70 50 y 0.0078125 0.015625 50 20y 0.00390625 0.0078125 20 20 0.015625 0.0625 70 50 y 0.0078125 0.0312570 50 y 0.00390625 0.015625 50 20 y Q.113 Pyraclostrobin Activity rateppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 70 0.25 50 2 2 90 70 y 1 2 90 70 y1 0.25 70 50 y 0.5 2 90 70 y Q.113 Chlorotalonil Activity rate ppm rateppm (%) P S? 1 0 0.5 0 0.25 0 0.25 20 1 0.25 50 20 y 0.5 0.25 70 20 y0.25 0.25 70 20 y Q.113 Flutriafol Activity rate ppm rate ppm (%) P S? 20 1 0 2 0 1 0 2 2 50 0 y 2 1 20 0 y 1 2 20 0 y Q.113 FludioxonilActivity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 00.0625 70 0.03125 0 0.25 0.03125 70 70 0.125 0.0625 20 0 y 0.125 0.0312590 70 y 0.0625 0.0625 90 70 y 0.0625 0.03125 20 0 y 0.03125 0.0625 20 0y Q.113 Fenpropimorph Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 00.25 0 0.125 0 0.5 70 0.25 0 0.125 0 2 0.5 100 70 y 1 0.5 100 70 y 10.25 100 0 y 0.5 0.5 100 70 y 0.5 0.25 70 0 y 0.5 0.125 20 0 y 0.25 0.5100 70 y 0.25 0.25 70 0 y 0.125 0.5 90 70 y 0.125 0.25 20 0 y CompoundQ.113 (VI) Activity rate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 00.03125 0 0.015625 0 0.0078125 0 0.0625 70 0.03125 70 0.015625 500.0078125 20 0.25 0.0625 90 70 y 0.125 0.0625 90 70 y 0.0625 0.0625 9070 y 0.03125 0.0625 90 70 y 0.015625 0.0625 90 70 y 0.015625 0.015625 7050 y 0.015625 0.03125 70 70 0.0078125 0.0078125 50 20 y 0.00781250.015625 70 50 y Q.113 Azoxystrobin Activity rate ppm rate ppm (%) P S?0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.25 20 0.125 0 0.5 0.125 20 0 y0.25 0.125 20 0 y 0.125 0.125 20 0 y 0.125 0.25 50 20 y 0.0625 0.125 200 y 0.0625 0.25 50 20 y 0.03125 0.125 20 0 y Q.113 PicoxystrobinActivity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 50 1 50 0.5 50 2 270 50 y 2 1 70 50 y 2 0.5 70 50 y 1 2 70 50 y 1 1 70 50 y 0.5 2 70 50 yQ.113 Trifloxystrobin Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 02 50 1 50 0.5 50 2 2 70 50 y 2 1 70 50 y 2 0.5 70 50 y 1 2 70 50 y 1 170 50 y 0.5 2 70 50 y Q.113 Prothioconazole Activity rate ppm rate ppm(%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.05 70 0.025 0 2 0.05 90 70 y 10.025 50 0 y 1 0.05 90 70 y 0.5 0.025 20 0 y 0.5 0.05 90 70 y 0.25 0.0250 0 0.25 0.05 100 70 y 0.125 0.025 20 0 y 0.125 0.05 90 70 y Q.113Propiconazole Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 00.125 0 0.5 50 0.25 0 2 0.5 70 50 y 1 0.25 20 0 y 1 0.5 70 50 y 0.5 0.2520 0 y 0.5 0.5 70 50 y 0.25 0.25 0 0 0.25 0.5 70 50 y 0.125 0.25 20 0 yQ.062 Fluxapyroxad Activity rate ppm rate ppm (%) P S? 0.03125 00.015625 0 0.0078125 0 0.00390625 0 0.125 70 0.0625 50 0.03125 500.015625 20 0.03125 0.0625 70 50 y 0.03125 0.125 90 70 y 0.015625 0.062570 50 y 0.0078125 0.03125 70 50 y 0.00390625 0.015625 50 20 y 0.00781250.015625 50 20 y Q.062 Pyraclostrobin Activity rate ppm rate ppm (%) PS? 2 0 1 0 0.5 0 2 70 2 2 90 70 y 1 2 90 70 y 0.5 2 90 70 y Q.062Chlorotalonil Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 0 0.2520 1 0.25 50 20 y 0.5 0.25 50 20 y 0.25 0.25 50 20 y Q.062 PicoxystrobinActivity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 2 50 1 50 0.5 50 2 270 50 y 2 1 70 50 y 2 0.5 70 50 y 1 2 70 50 y 1 1 70 50 y 1 0.5 70 50 y0.5 2 70 50 y 0.5 1 70 50 y Q.062 Fludioxonil Activity rate ppm rate ppm(%) P S? 0.25 0 0.1258 0 0.0625 0 0.03125 0 0.0625 50 0.03125 0 0.250.03125 90 50 y 0.125 0.0625 20 0 y 0.125 0.03125 90 50 y 0.0625 0.0625100 50 y 0.0625 0.03125 20 0 y 0.03125 0.0625 20 0 y .062Prothioconazole Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 00.125 0 0.05 50 0.025 0 2 0.05 100 50 y 1 0.025 50 0 y 1 0.05 100 50 y0.5 0.025 50 0 y 0.5 0.05 90 50 y 0.25 0.025 20 0 y 0.25 0.05 90 50 y0.125 0.025 20 0 y 0.125 0.05 90 50 y Q.062 Flutriafol Activity rate ppmrate ppm (%) P S? 2 0 1 0 0.5 0 2 0 1 0 0.5 0 2 2 50 0 y 2 1 20 0 y 20.5 20 0 y 1 2 20 0 y 0.5 2 20 0 y Q.062 Paclobutrazol Activity rate ppmrate ppm (%) P S? 1 0 0.5 0 0.25 0 0.125 0 5 70 2.5 0 1.25 0 1 5 100 70y 1 2.5 70 0 y 0.5 5 100 70 y 0.5 2.5 20 0 y 0.5 1.25 20 0 y 0.25 5 10070 y 0.125 5 100 70 y 0.125 2.5 100 0 y Q.062 Fenpropimorph Activityrate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.5 70 0.25 00.125 0 2 0.5 100 70 y 1 0.5 100 70 y 1 0.25 100 0 y 0.5 0.5 100 70 y0.5 0.25 70 0 y 0.5 0.125 20 0 y 0.25 0.5 100 70 y 0.25 0.25 70 0 y0.125 0.5 90 70 y 0.125 0.25 20 0 y Q.062 Procymidone Activity rate ppmrate ppm (%) P S? 0.125 0 0.0625 0 0.03125 0 0.015625 0 1.25 0 0.625 00.3125 0 0.125 1.25 70 0 y 0.0625 1.25 100 0 y 0.03125 1.25 90 0 y0.015625 0.625 70 0 y 0.015625 0.3125 50 0 y Q.062 PropiconazoleActivity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 0.25 0 0.125 0 0.5 500.25 0 2 0.5 90 50 y 1 0.25 50 0 y 1 0.5 70 50 y 0.5 0.25 20 0 y 0.5 0.570 50 y 0.25 0.25 0 0 0.25 0.5 70 50 y 0.125 0.25 20 0 y

Septoria tritici (Leaf Blotch)

Conidia of the fungus from cryogenic storage were directly mixed intonutrient broth (PDB potato dextrose broth). After placing a (DMSO)solution of the test compounds into a microtiter plate (96-well format)the nutrient broth containing the fungal spores was added. The testplates were incubated at 24° C. and the activity was determined visuallyafter 72 hrs.

Q.135 Fluxapyroxad Activity rate ppm rate ppm (%) P S? 0.03125 00.015625 0 0.0078125 0 0.00390625 0 0.0625 20 0.03125 0 0.015625 00.03125 0.0625 70 20 y 0.015625 0.03125 20 0 y 0.015625 0.0625 90 20 y0.0078125 0.03125 50 0 y 0.00390625 0.015625 20 0 y Q.135 Metconazole %rate ppm rate ppm Activity P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.062570 0.03125 0 0.25 0.0625 90 70 y 0.125 0.0625 90 70 y 0.125 0.03125 50 0y 0.0625 0.0625 100 70 y 0.0625 0.03125 20 0 y 0.03125 0.03125 20 0 yQ.135 Paclobutrazol Activity rate ppm rate ppm (%) P S? 1 0 0.5 0 0.25 00.125 0 5 50 2.5 0 1.25 0 0.625 0 1 2.5 50 0 y 1 5 70 50 y 0.5 5 90 50 y0.5 2.5 50 0 y 0.5 1.25 20 0 y 0.25 5 70 50 y 0.25 2.5 50 0 y 0.25 1.2520 0 y 0.25 0.625 20 0 y 0.125 5 70 50 y 0.125 2.5 50 0 y 0.125 1.25 200 y 0.125 0.625 20 0 y Q.135 Fluopyram Activity rate ppm rate ppm (%) PS? 1 0 0.5 0 0.25 0 0.25 50 1 0.25 90 50 y 0.5 0.25 70 50 y 0.25 0.25 7050 y Q.135 Prothioconazole Activity rate ppm rate ppm (%) P S? 0.5 00.25 0 0.125 0 0.0625 0 0.03125 0 0.0125 70 0.5 0.0125 90 70 y 0.250.0125 90 70 y 0.125 0.0125 90 70 y 0.0625 0.0125 90 70 y 0.03125 0.012590 70 y Q.135 Propiconazole Activity rate ppm rate ppm (%) P S? 0.5 00.25 0 0.125 0 0.0625 0 0.03125 0 0.125 50 0.5 0.125 90 50 y 0.25 0.12590 50 y 0.125 0.125 90 50 y 0.0625 0.125 90 50 y 0.03125 0.125 90 50 yQ.135 Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 1 00.5 0 2 1 90 0 y 2 0.5 50 0 y 1 1 70 0 y 1 0.5 20 0 y 0.5 1 50 0 y 0.50.5 20 0 y Q.135 Mandipropamid % rate ppm rate ppm Activity P S? 2 0 1 00.5 0 0.25 0 0.5 70 2 0.5 700 70 y 1 0.5 90 70 y 0.5 0.5 70 70 0.25 0.590 70 y Q.135 Penflufen Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.50 0.5 70 0.25 20 0.125 0 2 0.5 100 70 y 1 0.5 90 70 y 1 0.25 70 20 y 0.50.25 50 20 y 0.5 0.125 20 0 y Q.135 Fluazinam Activity rate ppm rate ppm(%) P S? 0.015625 0 0.0078125 0 0.00390625 0 0.03125 20 0.015625 00.015625 0.03125 50 20 y 0.0078125 0.03125 50 20 y 0.0078125 0.015625 200 y 0.00390625 0.015625 20 0 y Q.113 Fluxapyroxad Activity rate ppm rateppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 200.03125 0 0.015625 0 0.03125 0.0625 70 20 y 0.015625 0.03125 20 0 y0.015625 0.0625 90 20 y 0.0078125 0.03125 50 0 y 0.00390625 0.015625 200 y Q.113 Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 10 0.5 0 2 1 70 0 y 2 0.5 20 0 y 1 1 70 0 y 1 0.5 20 0 y 0.5 1 70 0 y 0.50.5 20 0 y Q.113 Paclobutrazol Activity rate ppm rate ppm (%) P S? 0.5 00.125 0 0.0625 0 0.03125 0 0.015625 0 2.5 50 0.625 0 0.3125 20 0.15625 00.5 2.5 90 50 y 0.125 2.5 70 0 y 0.0625 0.625 70 50 y 0.03125 0.15625 200 y 0.015625 0.3125 70 20 y Q.113 Picoxystrobin Activity rate ppm rateppm (%) P S? 0.0078125 0 0.00390625 0 0.03125 90 0.015625 70 0.007812550 0.0078125 0.03125 90 70 y 0.0078125 0.015625 90 70 y 0.003906250.0078125 70 50 y Q.113 Fluazinam Activity rate ppm rate ppm (%) P S?0.015625 0 0.0078125 0 0.00390625 0 0.03125 20 0.015625 0 0.0156250.03125 50 20 y 0.0078125 0.03125 50 20 y 0.0078125 0.015625 20 0 y0.00390625 0.015625 20 0 y Q.113 Fludioxonil Activity rate ppm rate ppm(%) P S? 1 0 0.5 0 0.25 0 0.25 70 1 0.25 90 70 y 0.5 0.25 90 70 y 0.250.25 90 70 y Q.113 Prothioconazole Activity rate ppm rate ppm (%) P S?0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0125 70 0.5 0.0125 90 70 y0.25 0.0125 90 70 y 0.125 0.0125 90 70 y 0.0625 0.0125 90 70 y 0.031250.0125 90 70 y Q.113 Propiconazole Activity rate ppm rate ppm (%) P S?0.5 0 0.25 0 0.125 0 0.0625 0 0.03125 0 0.125 50 0.5 0.125 90 50 y 0.250.125 70 50 y 0.125 0.125 70 50 y 0.0625 0.125 70 50 y 0.03125 0.125 7050 y Q.062 Isopyrazam Activity rate ppm rate ppm (%) P S? 0.0078125 00.00390625 0 0.03125 20 0.015625 0 0.0078125 0.03125 70 20 y 0.003906250.015625 70 0 y Q.062 Fluxapyroxad Activity rate ppm rate ppm (%) P S?0.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 20 0.03125 00.015625 0 0.03125 0.0625 70 20 y 0.015625 0.03125 20 0 y 0.0156250.0625 90 20 y 0.0078125 0.03125 70 0 y 0.00390625 0.015625 20 0 y Q.062Flutriafol Activity rate ppm rate ppm (%) P S? 2 0 1 0 0.5 0 1 0 0.5 0 21 70 0 y 2 0.5 20 0 y 1 1 70 0 y 1 0.5 20 0 y 0.5 1 70 0 y Q.062Picoxystrobin Activity rate ppm rate ppm (%) P S? 0.03125 0 0.015625 00.0078125 0 0.00390625 0 0.015625 70 0.0078125 20 0.03125 0.0078125 5020 y 0.015625 0.0078125 20 20 0.0078125 0.0078125 70 20 y 0.00781250.0015625 100 70 y 0.00390625 0.0078125 90 20 y Q.062 Fluazinam Activityrate ppm rate ppm (%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.00390625 00.0625 70 0.03125 20 0.015625 0 0.03125 0.0625 90 70 y 0.015625 0.062590 70 y 0.015625 0.03125 50 20 y 0.0078125 0.03125 50 20 y 0.00781250.015625 20 0 y 0.00390625 0.015625 20 0 y Q.062 Metconazole Activityrate ppm rate ppm (%) P S? 0.25 0 0.125 0 0.0625 0 0.03125 0 0.0625 500.25 0.0625 70 50 y 0.125 0.0625 70 50 y 0.0625 0.0625 70 50 y 0.031250.0625 70 50 y Q.062 Paclobutrazol Activity rate ppm rate ppm (%) P S? 10 0.5 0 0.25 0 10 70 5 70 2.5 20 1.25 0 0.625 0 1 2.5 50 20 y 0.5 10 10070 y 0.5 2.5 70 20 y 0.5 1.25 20 0 y 0.25 10 100 70 y 0.25 5 100 70 y0.25 2.5 70 20 y 0.25 0.625 90 0 y Q.062 Fluopyram Activity rate ppmrate ppm (%) P S? 0.125 0 0.0625 0 0.03125 0 0.25 50 0.125 0 0.125 0.2570 50 y 0.0625 0.25 70 50 y 0.0625 0.125 20 0 y 0.03125 0.125 20 0 yQ.062 Prothioconazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 00.125 0 0.0625 0 0.03125 0 0.0125 70 0.5 0.0125 90 70 y 0.25 0.0125 9070 y 0.125 0.0125 90 70 y 0.0625 0.0125 90 70 y 0.03125 0.0125 90 70 yQ.062 Propiconazole Activity rate ppm rate ppm (%) P S? 0.5 0 0.25 00.125 0 0.0625 0 0.03125 0 0.125 50 0.5 0.125 90 50 y 0.25 0.125 90 50 y0.125 0.125 90 50 y 0.0625 0.125 70 50 y 0.03125 0.125 70 50 y

Gaeumannomvces graminis (Take-all of Cereals)

Mycelial fragments of the fungus from cryogenic storage were directlymixed into nutrient broth (PDB potato dextrose broth). After placing a(DMSO) solution of the test compounds into a microtiter plate (96-wellformat) the nutrient broth containing the fungal spores was added. Thetest plates were incubated at 24° C. and the activity was determinedvisually after 48 hrs

Compound (V) Activity rate ppm (%) P S? Q.113 rate ppm 0.25 0 0.125 00.0625 0 0.03125 0 0.015625 0 0.0625 70 0.03125 20 0.015625 0 0.250.0625 90 70 y 0.125 0.03125 50 20 y 0.0625 0.015625 20 0 y 0.06250.03125 50 20 y 0.03125 0.0625 90 70 y 0.015625 0.03125 50 20 y Q.062rate ppm 0.015625 0 0.0078125 0 0.00390625 0 0.0625 70 0.03125 200.015625 0 0.015625 0.03125 50 20 y 0.0078125 0.015625 20 0 y 0.0156250.0625 100 70 y 0.0078125 0.03125 70 20 y 0.00390625 0.015625 20 0 y

Pythium ultimum (Damping Off):

Mycelial fragments of the fungus, prepared from a fresh liquid culture,were directly mixed into nutrient broth (PDB potato dextrose broth).After placing a (DMSO) solution of the test compounds into a microtiterplate (96-well format) the nutrient broth containing the fungal sporeswas added. The test plates were incubated at 24° C. and the activity wasdetermined visually after 48 hrs

Q.135 Mefenoxam Activity rate ppm rate ppm (%) P S? 0.0625 0 0.03125 00.015625 0 0.0078125 0 0.03125 50 0.0625 0.03125 70 50 y 0.03125 0.0312550 50 0.015625 0.03125 70 50 y 0.0078125 0.03125 70 50 y

Mycosphaerella arachidis (y. Cercospora arachidicola),

Brown leaf spot of groundnut (peanut): Conidia of the fungus fromcryogenic storage were directly mixed into nutrient broth (PDB potatodextrose broth). After placing a (DMSO) solution of the test compoundsinto a microtiter plate (96-well format) the nutrient broth containingthe fungal spores was added. The test plates were incubated at 24° C.and activity was determined visually after 5-6 days.

Q.135 Sedaxan Activity rate ppm rate ppm (%) P S? 0.0625 50 0.03125 500.015625 20 0.0078125 0 0.03125 0 0.015625 0 0.00390625 0 0.0625 0.0312570 50 y 0.0625 0.015625 70 50 y 0.03125 0.031215 50 50 0.0156250.00390625 50 20 y 0.0078125 0.00390625 20 0 y Q.135 Fluazinam Activityrate ppm rate ppm (%) P S? 0.0625 50 0.03125 50 0.15625 0 0.0078125 00.03125 0 0.015625 0 0.0078125 0 0.00390625 0 0.0625 0.015625 70 50 y0.03125 0.015625 50 50 y 0.015625 0.03125 20 0 y 0.015625 0.015625 20 0y 0.015625 0.0078125 50 0 y 0.015625 0.00390625 50 0 y 0.0078125 0.0312520 0 y 0.0078125 0.00390625 20 0 y Q.135 Cyprodinil % rate ppm rate ppmActivity P S? 0.03125 50 0.015625 20 0.00125 0 0.0625 0 0.003125 00.0015625 0 0.00078125 0 0.03125 0.00078125 90 50 y 0.03125 0.0015625 7050 y 0.03125 0.003125 70 50 y 0.03125 0.00625 70 50 y 0.03125 0.0125 7050 y 0.015625 0.00078125 50 20 y Q.135 Fludioxonil Activity rate ppmrate ppm (%) P S? 0.03125 50 0.015625 20 0.0625 0 0.03125 0 0.015625 00.0078125 0 0.00390625 0 0.03125 0.015625 70 50 y 0.015625 0.0625 50 20y 0.015625 0.03125 50 20 y 0.015625 0.015625 50 20 y 0.015625 0.007812550 20 y 0.015625 0.00390625 50 20 y Q.135 Fenpropimorph Activity rateppm rate ppm (%) P S? 0.0625 70 0.03125 70 0.015625 70 0.0078125 200.00390625 0 0.03125 70 0.015625 50 0.0078125 20 0.00390625 20 0.06250.015625 100 85 y 0.03125 0.015625 100 85 y 0.015625 0.0078125 90 76 y0.015625 0.00390625 90 76 y 0.0078125 0.03125 100 76 y 0.00781250.0078125 50 36 y 0.0078125 0.00390625 50 36 y 0.00390625 0.015625 70 50y 0.00390625 0.0078125 50 20 y Q.113 Sedaxan Activity rate ppm rate ppm(%) P S? 0.125 20 0.0625 0 0.125 0 0.0625 0 0.03125 0 0.015625 0 0.1250.125 50 20 y 0.0625 0.125 20 0 y 0.0625 0.0625 20 0 y 0.0625 0.03125 200 y 0.0625 0.015625 20 0 y Q.113 Fluazinam Activity rate ppm rate ppm(%) P S? 0.03125 0 0.015625 0 0.0078125 0 0.0625 20 0.03125 0 0.031250.0625 50 20 y 0.015625 0.0625 50 20 y 0.0078125 0.03125 20 0 y Q.113Fludioxonil Activity rate ppm rate ppm (%) P S? 0.5 70 0.25 70 0.125 500.0625 20 0.03125 0 0.5 70 0.25 0 0.125 0 0.5 0.25 100 70 y 0.25 0.25 9070 y 0.125 0.5 100 85 y 0.125 0.25 70 50 y 0.0625 0.25 50 20 y 0.031250.125 20 0 y Q.113 Fenpropimorph Activity rate ppm rate ppm (%) P S?0.125 50 0.0625 50 0.03125 20 0.015625 0 0.0625 70 0.03125 50 0.1250.0625 100 85 y 0.125 0.03125 100 75 y 0.0625 0.03125 90 75 y 0.031250.0625 100 76 y 0.015625 0.03125 70 50 y Q.062 Bixafen Activity rate ppmrate ppm (%) P S? 0.0625 0 0.03125 0 0.015625 0 0.0625 70 0.03125 500.0625 0.0625 90 70 y 0.03125 0.0625 90 70 y 0.015625 0.0625 100 70 y0.015625 0.03125 70 50 y Q.062 Fludioxonil Activity rate ppm rate ppm(%) P S? 2 70 1 70 0.5 0 0.25 0 0.125 0 0.5 50 0.25 0 0.125 0 2 0.5 10085 y 1 0.5 100 85 y 0.5 0.5 100 50 y 0.5 0.25 50 0 y 0.5 0.125 20 0 y0.25 0.5 70 50 y 0.25 0.25 20 0 y 0.125 0.25 20 0 y Q.062 CyprodinilActivity rate ppm rate ppm (%) P S? 1 70 0.2 0 0.1 0 0.05 0 0.025 0 10.025 90 70 y 1 0.1 90 70 y 1 0.2 90 70 y

Septoria tritici (Leaf Blotch):

After placing solutions of the test compounds (containing 0.2% DMSO)into a microtiter plate (96-well format), an equal amount of thenutrient broth (YBG) was added to each of the well. Finally the fungalspore solution was added. The test plates were incubated at 20° C. Theinhibition of growth was determined photometrically after 6 days and theactivity calculated in relation to untreated control.

Q.135 Tebuconazole Activity rate ppm rate ppm (%) P S? 1.25 24 0.625 250.3125 35 1.25 0 1.25 1.25 59 24 y 0.625 1.25 51 25 y 0.3125 1.25 54 35y Q.135 Epoxiconazole % rate ppm rate ppm Activity P S? 1.25 22 0.625 320.3125 34 0.15625 29 0.3125 78 0.15625 65 1.25 0.3125 95 83 y 0.6250.3125 98 85 y 0.625 0.15625 94 76 y 0.3125 0.3125 100 86 y 0.156250.3125 100 85 y 0.15625 0.15625 98 75 y Q.113 Cyproconazole Activityrate ppm rate ppm (%) P S? 10 63 1 84 0.5 64 0.25 0 10 1 100 94 y 10 0.5100 87 y 10 0.25 86 63 y Q.113 Prothioconazole Activity rate ppm rateppm (%) P S? 0.15625 42 0.078125 31 0.0390625 28 0.01953125 15 0.039062563 0.01953125 69 0.15625 0.0390625 96 78 y 0.078125 0.0390625 100 74 y0.078125 0.01953125 100 79 y 0.0390625 0.0390625 99 73 y 0.019531250.0390625 100 68 y 0.01953125 0.01953125 93 74 y Q.113 EpoxiconazoleActivity rate ppm rate ppm (%) P S? 1.25 42 0.625 39 0.3125 34 0.1562534 0.078125 33 0.3125 50 1.25 0.3125 97 71 y 0.625 0.3125 100 70 y0.3125 0.3125 99 67 y 0.15625 0.3125 99 67 y 0.078125 0.3125 98 67 yQ.062 Cyproconazole Activity rate ppm rate ppm (%) P S? 5 64 2.5 49 1.2548 2.5 76 1.25 39 5 1.25 96 78 y 2.5 2.5 100 88 y 2.5 1.25 86 69 y 1.252.5 98 88 y 1.25 1.25 87 69 y Q.062 Prothioconazole Activity rate ppmrate ppm (%) P S? 0.3125 33 0.15625 38 0.0078125 31 0.0625 63 0.03125 90.3125 0.0625 88 75 y 0.15625 0.0625 98 77 y 0.078125 0.03125 63 37 yQ.062 Tebuconazole Activity rate ppm rate ppm (%) P S? 5 57 2.5 41 1.2551 5 73 2.5 47 5 5 100 89 y 5 2.5 96 77 y 2.5 5 100 84 y 2.5 2.5 81 69 y1.25 5 99 87 y Q.062 Prochloraz Activity rate ppm rate ppm (%) P S?0.625 35 0.3125 37 0.03125 80 0.015625 48 0.625 0.03125 98 87 y 0.6250.015625 79 66 y 0.3125 0.03125 97 87 y Q.062 Epoxiconazole Activityrate ppm rate ppm (%) P S? 2.5 48 1.25 51 0.625 48 0.3125 42 0.625 710.3125 33 2.5 0.625 98 85 y 1.25 0.3125 77 67 y 0.625 0.3125 79 65 y0.3125 0.3125 71 61 y Q.062 Difenoconazole Activity rate ppm rate ppm(%) P S? 0.625 40 0.3125 36 0.15625 39 0.078125 29 0.00390625 32 0.1562548 0.625 0.15625 89 69 y 0.3125 0.15625 81 67 y 0.15625 0.15625 77 68 y0.078125 0.15625 81 63 y 0.00390625 0.15625 84 64 y Compound Q.062(S)-(VII) Activity rate ppm rate ppm (%) P S? 0.625 26 0.3125 22 0.12562 0.0625 44 0.03125 0

Sclerotinia sclerotiorum on Oilseed Rape, Preventive Treatment

The compound activity was tested under 1 day preventive conditions.Oilseed rape plants with 3 unfolded leafs were sprayed with a tracksprayer and 200 I/ha spray volume with the test compounds, either soloor in tankmix as shown in the table below.

1 day after application the plants were infested with a solution ofSclerotinia sclerotiorum mycelium. The plants were placed under plastichoods and high humidity conditions in a climate chamber at 14 h day/10 hnight cycle and 15° C. Disease infestation was evaluated visually 11days after application and average activity calculated in relation todisease severity on untreated check.

Boscalid Activity rate g a.i./ha (%) P S? Q.135 rate ppm 100 15 50 0 250 100 25 50 8 100 100 59 36 y 50 50 49 8 y 25 100 76 25 y 100 50 62 21 y50 50 92 10 y 25 100 83 25 y 100 50 93 32 y Q.113 rate ppm 100 39 50 225 2 100 25 50 8 100 100 83 54 y 50 50 89 10 y 25 100 83 26 y 100 50 8644 y Q.062 rate ppm 100 26 50 2 25 0 100 25 50 8 100 100 91 44 y 50 5092 10 y 25 100 83 25 y 100 50 93 32 y

Sphaerotheca fuliqinea (Powdery Mildew) on Cucumber, PreventiveTreatment

The compound activity was tested under 2 days preventive conditions.Cucumber plants with unfolded cotyledons were sprayed with a roomsprayerand 40 ml/4 plants spray volume with the test compounds, either solo orin tankmix as shown in the table below.

2 days after application the plants were infested with spores ofSphaerotheca fuliginea. The plants were placed in a climate chamberunder 70% rel. humidity, 22° C. and 14 h day/10 h night cycle. Diseaseinfestation was evaluated visually 10 days after application and averageactivity calculated in relation to disease severity on untreated check.

Acibenzolar-s- methyl Activity rate ppm (%) P S? Q.135 rate ppm 2 0 0.60 0.2 0 20 4 6 0 2 0 0.6 0 2 20 49 4 y 2 6 16 0 y 0.6 6 15 0 y 0.6 2 4 00.2 2 3 0 Q.113 rate ppm 2 0 0.6 0 0.2 0 20 4 6 0 2 0 0.6 0 2 20 18 4 y2 6 12 0 y 0.6 6 5 0 0.6 2 7 0 0.2 2 9 0 y Q.062 rate ppm 2 7 0.6 0 0.20 20 4 6 0 2 0 0.6 0 2 20 11 11 2 6 4 7 0.6 6 9 0 y 0.6 2 5 0 0.2 2 9 0y

Fusarium spp. on Wheat, Preventive Treatment

The compound activity was tested under 1 day preventive condition.Flowering wheat plants were sprayed with a track sprayer and 220 I/haspray volume with the test compounds, either solo or in tankmix as shownin the table below. The compounds were formulated as standard EC100 anddiluted into water to the given spray-dosis.

1 day after application the flowering ears were infested with a mix ofspores of Fusarium graminearum and Fusarium culmorum. The plants wereplaced in a climate chamber under 60% rel. humidity, and 14 h day/10 hnight cycle with 23/21° C. Disease infestation was evaluated visually 9days after application and average activity calculated in relation todisease severity on untreated check.

Activity Compound g a.i./ha (%) P S? Prothioconazole (PTZ)  50 55 Q.062200 17 Q.135 200 28 Q.113 200 23 Q.151 200 3 PTZ + Q.062 200 + 50 83 63y PTZ + Q.135 200 + 50 86 68 y PTZ + Q.113 200 + 50 85 65 y PTZ + Q.151200 + 50 88 56 y

Phakopsora pachyrhizi on Soybean, Preventive Treatment

The compound activity was tested under 1 day preventive conditions.Soybean plants with a fully enfolded first trifoliate leaf were sprayedwith a track sprayer and 50 I/ha spray volume with the test compounds,either solo or in tankmix as shown in the table below. 1 day afterapplication leaf discs were cutted from the first trifoliate leaf andplaced in multiwell plates on water-agar. 5 leaf discs per treatmentwhere infested with spores of a triazole tolerant soybeanrust strain.The multiwell plates where sealed and placed in an incubator 48 h indarkness and 12 h light/dark cycle afterwards. Rust infestation on leafdiscs was evaluated visually 11 days after application and averageactivity calculated in relation to disease severity on untreated checkleaf discs.

Rate Activity Compound (g ai/ha) (%) P S? Cyproconazole 2 53 N/A N/ACyproconazole   0.5 38 N/A N/A Q.062 2 13 N/A N/A Q.062   0.5 0 N/A N/AQ.063 2 0 N/A N/A Q.063   0.5 0 N/A N/A Q.113 2 25 N/A N/A Q.113   0.5 1N/A N/A Q.135 2 41 N/A N/A Q.135   0.5 13 N/A N/A Q.062 + 2 + 2 99 59Yes Cyproconazole Q.062 +  2 + 0.5 78 46 Yes Cyproconazole Q.062 + 0.5 +2  96 53 Yes Cyproconazole Q.063 + 2 + 2 100 53 Yes CyproconazoleQ.063 +  2 + 0.5 98 38 Yes Cyproconazole Q.063 + 0.5 + 2  98 53 YesCyproconazole Q.113 + 2 + 2 100 65 Yes Cyproconazole Q.113 +  2 + 0.5 9454 Yes Cyproconazole Q.113 + 0.5 + 2  96 54 Yes Cyproconazole Q.135 +2 + 2 95 72 Yes Cyproconazole Q.135 +  2 + 0.5 98 72 Yes CyproconazoleQ.135 + 0.5 + 2  97 46 Yes Cyproconazole

Septoria tritici on Wheat, Preventive Treatment

Four pots per treatment with 4 plants of the wheat variety Riband ineach of 6.5 cm pots have been treated 14 days after sowing with thecompounds given in the results table. The compounds were formulated asstandard EC100 and diluted into water to the given spray-dosis. One dayafter application of the compounds solo and in mixture, the plants wereinfested with spores of Septoria tritici. To enable a good infestation,the plants were covered with a plexiglas hood for 48 h afterinoculation. The plants grew in a controlled environment for 14 h at 21°C. during day and 10 h at 19° C. during night. 18 days after applicationthe infestation of the 2^(nd) leaf of each of the plants and of theuntreated, infested check was evaluated visually. The activity data inthe table then derived from a calculation of the infestation of themeans of the 4 plants of 4 repetitions of each of the solo or mixturetreatments with the mean of the of the 4 plants of 4 repetitions of theuntreated infested check.

Activity ga/ha (%) P S? compound (VII) 27  96 N/A N/A 9 20 3 0 Q.062 27 71 N/A N/A 9 8 3 6 Q.135 27  82 N/A N/A 9 33 3 0 Q.113 27  16 N/A N/A 90 3 0 Q.151 27  0 N/A N/A 9 0 3 0 compound (VII) +  9 + 27 98 77 Y Q.0623 + 9 36 8 Y compound (VII) + 27 + 27 99 99 Q.062 9 + 9 93 26 Y compound(VII) + 27 + 9  97 97 Q.062 9 + 3 58 25 Y compound (VII) +  9 + 27 98 47Y Q.135 3 + 9 47 0 Y compound (VII) + 27 + 27 100 99 Q.135 9 + 9 92 47 Ycompound (VII) + 27 + 9  100 98 Q.135 9 + 3 91 20 Y compound (VII) + 9 + 27 97 33 Y Q.113 3 + 9 38 0 Y compound (VII) + 27 + 27 100 97 Q.1139 + 9 76 20 Y compound (VII) + 27 + 9  99 96 Q.113 9 + 3 70 20 Ycompound (VII) +  9 + 27 97 20 Y Q.151 3 + 9 69 0 Y compound (VII) +27 + 27 99 96 Q.151 9 + 9 96 20 Y compound (VII) + 27 + 9  99 96 Q.1519 + 3 71 20 Yes Activity Compound g a.i./ha (%) P S? Difenoconazole 27 5(DFZ) 9 3 3 0 1 0 0.33 0 Q.062 81 61 27 50 9 26 3 8 1 2 Q.135 81 70 2752 9 43 3 9 1 0 Q.113 81 53 27 61 9 29 3 0 1 1 Q.151 81 43 27 13 9 0 3 41 0 DFZ + 27 + 81 97 63 Y Q.062  9 + 27 49 51 27 + 27 85 52 Y 9 + 9 2128 27 + 9  61 30 Y 9 + 3 0 10 DFZ + 27 + 81 100 71 Y Q.135  9 + 27 92 54Y 27 + 27 90 55 Y 9 + 9 42 45 27 + 9  68 46 Y 9 + 3 41 12 Y DFZ + 27 +81 98 56 Y Q.113  9 + 27 94 62 Y 27 + 27 95 63 Y 9 + 9 69 31 Y 27 + 9 91 32 Y 9 + 3 50 3 Y DFZ + 27 + 81 94 46 Y Q.151  9 + 27 68 15 Y 27 + 2797 17 Y 9 + 9 64 3 Y 27 + 9  85 5 Y 9 + 3 28 7 Y

What is claimed is:
 1. A fungicidal composition, comprising acombination of components A) and B), wherein component A) is a compoundof formula (I)

wherein R₁ and R₂ are each independently selected from hydrogen, C₁-C₄alkyl, C₃-C₄ alkenyl, C₃-C₄ alkynyl, (R₁₀)carbonyl and (R₁₀)oxycarbonyl;or R₁ and R₂ together with the nitrogen atom to which they are attachedform a 5- or 6 membered cyclic group which may be saturated orunsaturated and may contain a further heteroatom selected from S or O;R₃ represents hydrogen, halogen, cyano, nitro, mercapto, hydroxy,—C(═S)NH₂, —SF₅, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino,di(C₁-C₆alkyl)amino, a 5-membered heterocycle containing 1-4 nitrogenatoms, piperidino, morpholino, thiomorpholino, formyl, hydroxycarbonyl,C₂-C₇ alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ haloalkenyloxycarbonyl, C₂-C₇ alkylcarbonyl,C₂-C₇ haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆haloalkylsulfonyl, C₁-C₆ hydroxyalkyl, phenyl or benzyl wherein thephenyl and benzyl are optionally substituted by one or more groupsindependently selected from the group consisting of halogen, cyano,hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl; R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl,C₁-C₄ alkylsulfonyl, methylamino or dimethylamino; R₅ is hydrogen,C₁-C₁₂alkyl, C₃-C₁₂alkenyl, C₃-C₁₂alkynyl, C₁-C₁₂alkylsulfonyl,C₂-C₁₂alkenylsulfonyl, phenylsulfonyl or benzylsulfonyl, or isC₁-C₁₂alkyl, C₂-C₁₂alkenyl, C₂-C₁₂alkynyl, C₁-C₁₂alkylsulfonyl,C₂-C₁₂alkenylsulfonyl, phenylsulfonyl or benzylsulfonyl mono- topolysubstituted by substituents independently selected from the groupconsisting of halogen, cyano, nitro, hydroxy, mercapto, azido, formyl,C₂-C₇alkylcarbonyl, C₂-C₇haloalkylcarbonyl, C₁-C₆alkyl, C₁-C₆haloalkyl,C₁-C₆alkoxy, C₁-C₆haloalkoxy, C₁-C₆alkylthio, C₁-C₆alkylsulfinyl andC₁-C₆alkylsulfonyl; or R₅ is formyl, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂alkenylcarbonyl, C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂ cycloalkylcarbonyl,benzylcarbonyl, phenylcarbonyl, C₂-C₁₂ alkoxycarbonyl, C₄-C₁₂alkenyloxycarbonyl, C₄-C₁₂ alkynyloxycarbonyl, C₄-C₁₂cycloalkoxycarbonyl, benzyloxycarbonyl or phenoxycarbonyl, or is C₂-C₁₂alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, C₃-C₁₂ alkynylcarbonyl, C₄-C₁₂cycloalkylcarbonyl, benzylcarbonyl, phenylcarbonyl, C₂-C₁₂alkoxycarbonyl, C₄-C₁₂ alkenyloxycarbonyl, C₄-C₁₂ alkynyloxycarbonyl,C₄-C₁₂ cycloalkoxycarbonyl, benzyloxycarbonyl or phenoxycarbonyl mono-to polysubstituted by substituents independently selected from the groupconsisting of halogen, cyano, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆alkoxy; or R₅ is (R₅₁)(R₅₂)(R₅₃)Si—, (R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-,(R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-, (R₅₄O)(R₅₅O)(R₅₆O)Si—,(R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂ alkyl)- or (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₃-C₈cycloalkyl)-; or R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-,C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-,C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-,phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-,C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-,phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-,C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-,phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-,C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl- orphenyl-B—C₃-C₁₂cycloalkyl-, wherein the group B is selected from—C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—, —ON═C(R₆₀)—, —O—C(═O)—,—C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)2-, —S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—,—N═S(═O)(R₁₄)—, —N(R₆₂)—C═O)—, —C═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or—SO₂—N(R₆₂)—; or R₅ is C₁-C₆alkyl-B—C₁-C₁₂alkyl-,C₂-C₆alkenyl-B—C₁-C₁₂alkyl-, C₂-C₆alkynyl-B—C₁-C₁₂alkyl-,C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-, benzyl-B—C₁-C₁₂alkyl-,phenyl-B—C₁-C₁₂alkyl-, C₁-C₆alkyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-,C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-, benzyl-B—C₂-C₁₂alkenyl-,phenyl-B—C₂-C₁₂alkenyl-, C₁-C₆alkyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-,C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-, benzyl-B—C₂-C₁₂alkynyl-,phenyl-B—C₂-C₁₂alkynyl-, C₁-C₆alkyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-,C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-, benzyl-B—C₃-C₁₂cycloalkyl-,phenyl-B—C₃-C₁₂cycloalkyl-, all of which, in turn, are mono- topoly-substituted by substituents independently selected from the groupconsisting of halogen, cyano, hydroxy, mercapto, C₁-C₆ haloalkyl, C₁-C₆alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆ alkylsulfonyl; or R₅ is A-, A-(C₁-C₆alkyl)-,A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-, A-O—(C₄-C₆alkenyl)-,A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-, A-(C₃-C₈cycloalkyl)- orA-O—(C₃-C₈cycloalkyl)-; A is a three- to ten-membered monocyclic orfused bicyclic ring system which can be aromatic, partially saturated orfully saturated and can contain 1 to 4 hetero atoms selected from thegroup consisting of nitrogen, oxygen and sulphur, it not being possiblefor each ring system to contain —O—O—, —S—S— and —O—S— fragments, and itbeing possible for the three- to ten-membered ring system to be itselfmono- or polysubstituted A1) by substituents independently selected fromthe group consisting of halogen, cyano, nitro, hydroxy, mercapto, azido,formyl, carboxy, ═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl,C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl,C₃-C₈ halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy,C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, benzyl,benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy, phenyl andphenoxy, in turn, may be mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, cyano,nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl; or A2) by substituents independently selected form thegroup consisting of (R₁₄)S(═O)(═NR₁₃)—, (R₁₄)(R₁₅)S(═O)═N—;—Si(R₅₁)(R₅₂)(R₅₃), —NR₅₇R₅₈, —C(═O)NR₅₇R₅₈, —C(═S)NR₅₇R₅₈, HC(═NOR₅₉)—,(C₁-C₆alkyl)C(═NOR₅₉)—, (C₁-C₆haloalkyl)C(═NOR₅₉)—,(C₁-C₆alkyl)C(═NOR₅₉)C₁-C₆alkyl-, (C₁-C₆haloalkyl)C(═NOR₅₉)C₁-C₆alkyl-,N(C₁-C₆alkyl)aminosulfonyl and N,N-di(C₁-C₆alkyl)aminosulfonyl; or A3)by substituents independently selected from the group consisting offormyl, C₂-C₇ alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇alkenylcarbonyl, C₃-C₇ haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl,C₄-C₉ halocycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₂-C₇haloalkoxycarbonyl, C₃-C₇ al kenyloxycarbonyl, C₃-C₇ alkynyloxycarbonyl,C₄-C₉ cycloalkoxycarbonyl, C₂-C₇ alkylthiocarbonyl andbenzyloxycarbonyl, and benzyloxycarbonyl mono- to polysubstituted bysubstituents independently selected from the group consisting ofhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy;or A4) by substituents independently selected from the group consistingof hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl, phenyl,═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄ alkenyl, ═N—O—C₃-C₄alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄ haloalkenyl, ═N—O-benzyl and═N—O-phenyl, wherein the ═N—O-benzyl and ═N—O-phenyl are optionallysubstituted by one or more group selected from the group consisting ofhalogen, methyl, halomethyl; or R₅ is —N═C(R₈)(R₉); or R₅ is a C₈-C₁₁spirobicyclic system containing 0, 1 or 2 O or N atoms, wherein thereare no adjacent O atoms, which is optionally substituted by one or moregroups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH,tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl, C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂; or R⁵ is selected from G¹, G², G³-G⁴, G⁵,G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹², G¹³, G¹⁴, G¹⁵ and G¹⁶; R₆ is selected fromhydrogen and SH; R₇ is hydrogen, halogen or C₁-C₄ alkyl; R₈ and R₉,independently from each other, are hydrogen, halogen, cyano, C₁-C₁₂alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂ alkynyl, C₁-C₁₂ alkoxy, formyl, C₂-C₁₂alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl, carboxy, C₂-C₁₂ alkoxycarbonyland C₄-C₁₂ alkenyloxycarbonyl, or C₁-C₁₂ alkyl, C₂-C₁₂ alkenyl, C₂-C₁₂alkynyl, C₁-C₁₂ alkoxy, C₂-C₁₂ alkylcarbonyl, C₃-C₁₂ alkenylcarbonyl,C₂-C₁₂ alkoxycarbonyl and C₄-C₁₂ alkenyloxycarbonyl mono- topolysubstituted by substituents independently selected from the groupconsisting of halogen, cyano, nitro, hydroxy, mercapto, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆ alkylsulfonyl; or R₈ and R₉ together from aC₂-C₈ alkylene bridge which may optionally be mono- to polysubstitutedby substituents independently selected from the group consisting ofhalogen, cyano, C₁-C₆ alkyl and C₁-C₆ haloalkyl; or R₈ and R₉,independently from each other, are the groups A-, A-O— orA-(C₁-C₆alkyl)-; R₁₀ is H, C₁-C₄ alkyl, C₂-C₄ alkenyl or C₁-C₄haloalkyl; R₁₃ is hydrogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ alkenyl,C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈ cycloalkyl, C₃-C₈halocycloalkyl, phenyl and benzyl, or is phenyl and benzyl mono- topolysubstituted by halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkylor C₁-C₆ alkoxy; R₁₄ and R₁₅, independently of each other, are C₁-C₆alkyl, C₃-C₈ cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzylor phenyl independently of each other, substituted by substituentsselected from the group consisting of halogen, cyano, hydroxy, C₁-C₆alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; R₅₁, R₅₂, R₅₃, independently ofeach other, are halogen, cyano, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₃-C₈cycloalkyl, C₅-C₈ cycloalkenyl, C₂-C₆ alkynyl, C₁-C₆ alkoxy, benzyl orphenyl; R₅₄, R₅₅, R₅₆, independently of each other, are C₁-C₆ alkyl,C₃-C₆ alkenyl, C₃-C₈ cycloalkyl, C₃-C₆ alkynyl, benzyl or phenyl; R₅₇and R₅₈, independently of each other, are hydrogen, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈cycloalkyl, C₃-C₈ halocycloalkyl, phenyl or benzyl, where phenyl orbenzyl for their part may be mono- to polysubstituted on the phenyl ringby substituents independently selected from the group consisting ofhalogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy,or R₅₇ and R₅₈ together with their interconnecting nitrogen atom areaziridino, azetidino, pyrazolino, pyrazolidino, pyrrolino, pyrrolidino,imidazolino, imidazolidino, triazolino, tetrazolino, piperazino,piperidino, morpholino, thiomorpholino, each of which, in turn, may bemono- or polysubstituted by substituents selected from the groupconsisting of methyl, halogen, cyano; R₅₉ is hydrogen, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₃-C₆ alkenyl, C₃-C₆ haloalkenyl, C₃-C₆ alkynyl, C₃-C₈cycloalkyl, C₃-C₈ halocycloalkyl, benzyl and phenyl, and benzyl andphenyl mono- to polysubstituted by halogen, cyano, hydroxy, C₁-C₆ alkyl,C₁-C₆ haloalkyl or C₁-C₆ alkoxy; R₆₀ is hydrogen, C₁-C₆ alkyl, C₃-C₈cycloalkyl, C₁-C₆ haloalkyl, C₃-C₈ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, benzyl or phenyl, or benzyl or phenyl mono-to polysubstituted by substituents independently selected from the groupconsisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl andC₁-C₆ alkoxy; R₆₂ is hydrogen, C₁-C₆ alkyl, C₃-C₈ cycloalkyl, C₁-C₆haloalkyl, C₃-C₈ halocycloalkyl, C₃-C₆ alkenyl, C₃-C₆ alkynyl, benzyl orphenyl, or benzyl or phenyl mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, cyano,hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl and C₁-C₆ alkoxy; G¹ is a C₈-C₁₀fused bicyclic ring system which may be saturated or comprise onecarbon-carbon double bond and is optionally substituted by one or moregroups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy,halogen, C₁-C₄ haloalkyl and cyano; G² is C₃-C₆ cycloalkenyl, which isoptionally substituted by one or more groups independently selected fromhalogen, CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, ethyl,n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl,n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃,—CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆alkenyl, C₂-C₆haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl,C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂,—C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂; G³ is phenyl, which isoptionally substituted by one or more groups independently selected fromhydroxyl, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₁-C₄ alkoxy, halogen and cyano, wherein the alkyl groups are optionallysubstituted by one or more halogen; G⁴ is C₃-C₁₂ cycloalkyl which isoptionally substituted by one or more groups independently selected fromhydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen and cyano, wherein the alkyl groups are optionally substitutedby one or more halogen; G⁵ is C₃-C₇ cycloalkyl which is optionallysubstituted by one or more groups independently selected from halogen,CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH₂(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₃-C₆-alkenyloxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl,C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, phenoxy,—C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂; G⁶ is phenyl,which must be substituted by at least one fluorine and is optionallyfurther substituted by one or more groups independently selected fromhalogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl; G⁷ is methylene; G⁸ is

G⁹ is

G¹⁰ is phenyl, which is optionally substituted by one or more groupsindependently selected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl, C₁-C₆haloalkylsulfonyl, phenyl, 2-phenyl-ethynyl and 2-phenyl-ethyl; G¹¹ ismethylene substituted by at least one group independently selected fromC₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy; G¹²is

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, CN, NO₂, OH,SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl,C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆alkenyl, C₂-C₆ haloalkenyl,C₁-C₆alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂,—C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂; G¹⁴ is

G¹⁵ is

G¹⁶ is

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 to 4 members selected from the group consisting ofN, N(R^(69′)), O and S, it not being possible for each ring system tocontain —O—O—, —S—S— and —O—S— fragments, and it being possible for thefive- to six-membered ring system to be itself mono- or polysubstitutedby groups selected from the group consisting of halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy,C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl; R^(1′) is selected from the group consisting ofhydrogen fluorine C₁-C₄ alkyl, C₁-C₄ haloalkyl; R^(2′), R^(3′), R^(4′)and R^(5′) are selected, independently of each other, from the groupconsisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy and C₁-C₄ alkylthio; R^(11′), R^(12′), R^(13′) and R^(14′) areselected, independently of each other, from the group consisting ofhydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃),C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃),SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl,C₁-C₆alkoxy, C₁-C₆ haloalkoxy, phenyl, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, benzyloxy, C₁-C₆alkylthio, C₁-C₆ haloalkylthio,C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl andC₁-C₆ haloalkylsulfonyl; R^(15′) and R^(16′) are independently selectedfrom the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl and C₃-C₆ cycloalkyl; each R^(17′), R^(18′), R^(19′),R^(20′), R^(21′) and R^(22′) are selected independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl;R^(23′), R^(24′) and R^(25′) are independently selected from the groupconsisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄alkylthio; R^(26′) is C(R^(36′))₂, N—OH, N—O—C₁-C₄-alkyl,N—O—C₂-C₄-alkenyl, N—O—C₂-C₄ alkynyl, N—O—C₁-C₄ haloalkyl N—O—C₂-C₄haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O wherein theN—O-benzyl and N—O-phenyl may be substituted by one or more groupsindependently selected from the group consisting of halogen, methyl andhalomethyl; R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′),R^(33′), R^(34′) and R^(35′) are each independently selected from thegroup consisting of hydrogen, hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl,C₂-C₄ alkynyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄haloalkenyl, cyano, benzyl and phenyl; or R^(28′) and R^(29′) togetherwith the two carbon atoms to which they are attached form a double bond;each R^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl; R^(37′) and R^(38′) are selected independently of each other fromthe group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl and C₁-C₄haloalkyl; R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areselected independently of each other from the group consisting ofhydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio; R^(45′), R^(46′), R^(47′),R^(48′) and R^(49′) are selected, independently of each other, from thegroup consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂₁C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl; R^(50′) is selected from the group consisting ofhydrogen fluorine C₁-C₄ alkyl, C₁-C₄ haloalkyl; R^(51′), R^(52′),R^(53′), R^(54′), R^(55′) and R^(56′) are selected, independently ofeach other, from the group consisting of hydrogen fluorine C₁-C₄ alkyl,C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄ alkylthio; R^(57′), R^(58′),R^(59′) and R^(60′) are selected, independently of each other, from thegroup consisting of hydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₂-C₆ alkoxy, C₂-C₆ haloalkoxy, phenyl, C₃-C₆ alkenyloxy,C₃-C₆ haloalkynyl, C₃-C₆ alkynyloxy, C₃-C₆ alkynyloxy, C₃-C₆cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl; provided that at least one ofR^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen; R^(61′) andR^(62′) are selected independently of each other from the groupconsisting of hydrogen fluorine cyano C₁-C₄ alkyl and C₁-C₄ haloalkyl;R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) are selectedindependently of each other from the group consisting of hydrogen,halogen, hydroxy, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy, C₁-C₄haloalkoxy and C₁-C₄alkylthio; R^(69′) is selected from hydrogen C₁-C₄alkyl, C₃-C₄alkenyl and C₁-C₄ alkylcarboxy; n is 0 or 1; p and q areindependently selected from 0 and 1; and r, s and t are independentlyselected from 0 and 1; or an agronomically acceptable salt/metalliccomplex/metalloidic complex/isomer/structuralisomer/stereo-isomer/diastereoisomer/enantiomer/tautomer/N-oxidethereof; and component B) is a strobilurin fungicide, a sterolbiosynthesis inhibitor, a triazole fungicide, a pro-triazole fungicide,a DMI fungicide, a SDHI fungicide, or a compound selected from the groupconsisting of Chlorothalonil, Fludioxonil, Cyprodinil, Mandipropamid,Fluazinam, Procymedone, Carbendazim, Abamectin, Clothianidin, Emamectinbenzoate, Imidacloprid, Tefluthrin, Mefenoxam, Orocymedone,Thiamethoxam, Lambda-cyhalothrin, Gamma-cyhalothrin, Profenofos,Lufenuron, Diflubenzuron, Cypermethrin, Novaluron, Bifenthrin, Methomyl,Chlopyrifos, Methamidophos, Endosulfan, Betacyfluthrin, Triflumuron,Teflubenzuron, SulcotrioneAcephat, Glyphosate, Glufosinate, Mesotrione,Tembotrione, Sulcotrione, Auxins, Trinexapac-ethyl, Prohexadione-Ca,Paclobutrazol, Acibenzolar-S-methyl, Methyl-Jasmonate, Cis-Jasmone,Manganese, Cyflufenamid, Tebufloquin and Copper.
 2. A fungicidalcomposition according to claim 1, wherein component A) is a compound offormula (I) wherein, R₁ and R₂ are each independently selected fromhydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl and C₃-C₄ alkynyl; or R₁ and R₂together with the nitrogen atom to which they are connected formpyrrolidine or piperidine; R₃ represents hydrogen, halogen, cyano,mercapto, hydroxy, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄haloalkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₃-C₆cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino, pyrrolidino,imidazolino, triazolino, tetrazolino, formyl, C₂-C₅ alkylcarbonyl, C₂-C₅haloalkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆haloalkylsulfonyl or C₁-C₆ hydroxyalkyl; R₄ represents hydrogen,halogen, cyano, amino, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₃-C₆ cycloalkyl,C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄alkylthio, C₁-C₄ alkylsulfinyl, C₁-C₄ alkylsulfonyl, methylamino ordimethylamino; R₅ represents hydrogen, C₁-C₁₂ alkylsulfonyl, C₁-C₁₂alkyl, C₃-C₁₂ alkenyl, C₃-C₁₂ alkynyl, or is C₁-C₁₂ alkyl, C₂-C₁₂alkenyl, C₂-C₁₂ alkynyl mono- to polysubstituted by substituentsindependently selected from the group consisting of halogen, cyano,nitro, hydroxy, mercapto, azido, formyl, C₂-C₇ alkylcarbonyl, C₂-C₇haloalkylcarbonyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl; or R₅ is (R₅₁)(R₅₂)(R₅₃)Si—,(R₅₁)(R₅₂)(R₅₃)Si—(C₁-C₁₂alkyl)-, (R₅₁)(R₅₂)(R₅₃)Si—(C₃-C₈cycloalkyl)-,(R₅₄O)(R₅₅O)(R₅₆O)Si—, (R₅₄O)(R₅₅O)(R₅₆O)Si—(C₁-C₁₂alkyl)- or(R₅₄O)(R₅₅O)(R₅₆O)S(C₃-C₈cycloalkyl)-; or R₅ isC₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl- or phenyl-B—C₃-C₁₂cycloalkyl-, wherein thegroup B is selected from —C(═O)—, —C(═S)—, —C(═NOR₅₉)—, —C(R₆₀)═NO—,—ON═C(R₆₀)—, —O—C(═O)—, —C(═O)—O—, —O—, —S—, —S(═O)—, —S(═O)2-,—S(═O)(═NR₁₃)—, —S(═O)(R₁₄)═N—, —N═S(═O)(R₁₄)—, —N(R₆₂)—C(═O)—,—C(═O)—N(R₆₂)—, —N(R₆₂)—SO₂— or —SO₂—N(R₆₂)—; or R₅ isC₁-C₆alkyl-B—C₁-C₁₂alkyl-, C₂-C₆alkenyl-B—C₁-C₁₂alkyl-,C₂-C₆alkynyl-B—C₁-C₁₂alkyl-, C₃-C₈cycloalkyl-B—C₁-C₁₂alkyl-,benzyl-B—C₁-C₁₂alkyl-, phenyl-B—C₁-C₁₂alkyl-,C₁-C₆alkyl-B—C₂-C₁₂alkenyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkenyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkenyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkenyl-,benzyl-B—C₂-C₁₂alkenyl-, phenyl-B—C₂-C₁₂alkenyl-,C₁-C₆alkyl-B—C₂-C₁₂alkynyl-, C₂-C₆alkenyl-B—C₂-C₁₂alkynyl-,C₂-C₆alkynyl-B—C₂-C₁₂alkynyl-, C₃-C₈cycloalkyl-B—C₂-C₁₂alkynyl-,benzyl-B—C₂-C₁₂alkynyl-, phenyl-B—C₂-C₁₂alkynyl-,C₁-C₆alkyl-B—C₃-C₈cycloalkyl-, C₂-C₆alkenyl-B—C₃-C₈cycloalkyl-,C₂-C₆alkynyl-B—C₃-C₈cycloalkyl-, C₃-C₈cycloalkyl-B—C₃-C₈cycloalkyl-,benzyl-B—C₃-C₁₂cycloalkyl-, phenyl-B—C₃-C₁₂cycloalkyl-, all of which, inturn, are mono- to polysubstituted by substituents independentlyselected from the group consisting of halogen, cyano, hydroxy, mercapto,C₁-C₆ haloalkyl, C₁-C₆ alkoxy, formyl, C₂-C₆ alkylcarbonyl, C₁-C₆alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆ alkylsulfonyl; or R₅ isselected from A-, A-(C₁-C₆alkyl)-, A-O—(C₁-C₆alkyl)-, A-(C₃-C₆alkenyl)-,A-O—(C₄-C₆alkenyl)-, A-(C₃-C₆-alkynyl)-, A-O—(C₄-C₆alkynyl)-,A-(C₃-C₈cycloalkyl)- and A-O—(C₃-C₈cycloalkyl)-; A is a three- toten-membered monocyclic or fused bicyclic ring system which can bearomatic, partially saturated or fully saturated and can contain 1 to 4hetero atoms selected from the group consisting of nitrogen, oxygen andsulphur, it not being possible for each ring system to contain —O—O—,—S—S— and —O—S— fragments, and it being possible for the three- toten-membered ring system to be itself mono- or polysubstituted A1) bysubstituents independently selected from the group consisting ofhalogen, cyano, nitro, hydroxy, mercapto, nitro, azido, formyl, carboxy,═O, ═S, C₁-C₆ alkyl, C₂-C₆ alkenyl, C₂-C₆ alkynyl, C₃-C₈ cycloalkyl,C₁-C₆ haloalkyl, C₂-C₆ haloalkenyl, C₂-C₆ haloalkynyl, C₃-C₈halocycloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₈ cycloalkyloxy, C₃-C₈halocycloalkyloxy, C₃-C₈ cycloalkenyloxy, C₃-C₈ halocycloalkenyloxy,benzyl, benzyloxy, phenyl and phenoxy, where the benzyl, benzyloxy,phenyl and phenoxy, in turn, may be mono- to polysubstituted bysubstituents independently selected from the group consisting ofhalogen, cyano, nitro, hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl and C₁-C₆ alkylsulfonyl; or A3) by substituentsindependently selected from the group consisting of formyl, C₂-C₇alkylcarbonyl, C₂-C₇ haloalkylcarbonyl, C₃-C₇ alkenylcarbonyl, C₃-C₇haloalkenylcarbonyl, C₄-C₉ cycloalkylcarbonyl, C₂-C₇ alkoxycarbonyl,C₄-C₇ al kenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₄-C₉cycloalkoxycarbonyl and benzyloxycarbonyl, and benzyloxycarbonyl mono-to polysubstituted by substituents independently selected from the groupconsisting of halogen, cyano, hydroxy, C₁-C₆ alkyl, C₁-C₆ haloalkyl andC₁-C₆ alkoxy; or A4) by substituents independently selected from thegroup consisting of hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano,benzyl, phenyl, ═C(R^(36′))₂, ═N—OH, ═N—O—C₁-C₄-alkyl, ═N—O—C₃-C₄alkenyl, ═N—O—C₃-C₄ alkynyl, ═N—O—C₁-C₄ haloalkyl, ═N—O—C₃-C₄haloalkenyl, ═N—O-benzyl and ═N—O-phenyl, wherein the ═N—O-benzyl and═N—O-phenyl are optionally substituted by one or more group selectedfrom the group consisting of halogen, methyl, halomethyl; or R₅ is aC₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O, S or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, CN, NO₂, OH,SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇-alkylcarbonyl, C₂-C₇-alkoxycarbonyl, C₄-C₇-alkenyloxycarbonyl, C₄-C₇-alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂; R₆ is hydrogen; R₇ is hydrogen or C₁-C₄alkyl.
 3. A fungicidal composition according to claim 1, whereincomponent A) is a compound of formula (I) wherein R₁ and R₂ are eachindependently selected from hydrogen and C₁-C₄ alkyl; or R₁ and R₂together with the nitrogen atom to which they are connected formpyrrolidine or piperidine; R₃ represents hydrogen, halogen, cyano, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,C₃-C₆ cycloalkyl, amino, C₁-C₂ alkylamino, di(C₁-C₆alkyl)amino,pyrrolidino, imidazolino, triazolino, formyl, phenyl, C₂-C₄alkylcarbonyl, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonylor C₁-C₆ hydroxyalkyl; R₄ is selected from fluorine, chlorine, bromine,C₁-C₄ alkyl, C₁-C₄ alkenyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₃-C₆cycloalkyl; R₅ is selected from G¹, G², G³-G⁴, G⁵, G⁶-G⁷, G⁸, G⁹,G¹⁰-G¹¹, G¹², G¹³, G¹⁴, G¹⁵ and G¹⁶; R₆ is hydrogen; R₇ is selected fromhydrogen and C₁-C₄ alkyl; G¹ is a C₈-C₁₀ fused bicyclic ring systemwhich may be saturated or comprise one carbon-carbon double bond and isoptionally substituted by one or more groups independently selected fromhydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy, halogen, C₁-C₄ haloalkyl and cyano;G² is C₃-C₆ cycloalkenyl, which is optionally substituted by one or moregroups independently selected from halogen, CN, NO₂, OH, SH, CHO, COOH,tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl,sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₃-C₆halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇ alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl, C₁-C₆ alkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ alkylsulfonyl, —C(═O)NH₂, —C(═O)NH(CH₃),—C(═O)N(CH₃)₂ and —C(═S)NH₂; G³ is phenyl, which is optionallysubstituted by one or more groups independently selected from hydroxyl,C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄alkoxy, halogen and cyano, wherein the alkyl groups are optionallysubstituted by one or more halogen; G⁴ is C₃-C₁₂ cycloalkyl which isoptionally substituted by one or more groups independently selected fromhydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen and cyano, wherein the alkyl groups are optionally substitutedby one or more halogen; G⁵ is C₃-C₇ cycloalkyl, which is optionallysubstituted by one or more groups independently selected from halogen,CN, NO₂, OH, SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₁-C₆ alkoxy,C₁-C₆ haloalkoxy, C₃-C₆-alkenyloxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄-C₇ al kenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl,C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, phenoxy,—C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂; G⁶ is phenyl,which must be substituted by at least one fluorine and is optionallyfurther substituted by one or more groups independently selected fromhalogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl; G⁷ is methylene; G⁸ is

G⁹ is

G¹⁰ is phenyl, which is optionally substituted by one or more groupsindependently selected from halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, phenyl, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl, C₁-C₆haloalkylsulfonyl, phenyl, 2-phenyl-ethynyl and 2-phenyl-ethyl; G¹¹ ismethylene substituted by at least one group independently selected fromC₁-C₄ alkyl, C₁-C₄ haloalkyl, CN, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy; G¹²is

G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms,wherein there are no adjacent O atoms, which is optionally substitutedby one or more groups independently selected from halogen, CN, NO₂, OH,SH, CHO, COOH, tri(C₁-C₆-alkyl)silyl, C₁-C₆ alkyl, C₁-C₆ haloalkyl,C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₂-C₇ alkylcarbonyl, C₂-C₇alkoxycarbonyl, C₄-C₇ alkenyloxycarbonyl, C₄-C₇ alkynyloxycarbonyl,C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ alkylsulfonyl, ═O,—C(═O)NH₂, —C(═O)NH(CH₃), —C(═O)N(CH₃)₂ and —C(═S)NH₂; G¹⁴ is

G¹⁵ is

G¹⁶ is

G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 to 4 members selected from the group consisting ofN, N(R⁶⁹), O and S, it not being possible for each ring system tocontain —O—O—, —S—S— and —O—S— fragments, and it being possible for thefive- to six-membered ring system to be itself mono- or polysubstitutedby groups selected from the group consisting of halogen, CN, NO₂, OH,SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃),C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy,C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl; R^(1′) is selected from the group consisting ofhydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl; R^(2′), R^(3′), R^(4′)and R^(5′) are selected, independently of each other, from the groupconsisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄alkoxy and C₁-C₄ alkylthio; R^(11′), R^(12′), R^(13′) and R^(14′) areselected, independently of each other, from the group consisting ofhydrogen, halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃),C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃),SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆alkoxy, C₁-C₆ haloalkoxy, phenyl, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, benzyloxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl; R^(15′) and R^(16′) are independently selected fromthe group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄haloalkyl and C₃-C₆ cycloalkyl; each R^(17′), R^(18′), R^(19′), R^(20′),R^(21′) and R^(22′) are selected independently of each other, from thegroup consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₃-C₆ cycloalkyl; R^(23′),R^(24′) and R^(25′) are independently selected from the group consistingof hydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy,C₃-C₆ cycloalkyl, C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio; R^(26′) isC(R^(36′))₂, N—OH, N—O—C₁-C₄-alkyl, N—O—C₂-C₄-alkenyl, N—O—C₂-C₄alkynyl, N—O—C₁-C₄ haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl,N—O-phenyl, N—O-halophenyl, O wherein the N—O-benzyl and N—O-phenyl maybe substituted by one or more groups independently selected from thegroup consisting of halogen, methyl and halomethyl; R^(27′), R^(28′),R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′) and R^(35′) areeach independently selected from the group consisting of hydrogen,hydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen, C₁-C₄ haloalkyl, C₂-C₄ haloalkenyl, cyano, benzyl and phenyl;or R^(28′) and R^(29′) together with the two carbon atoms to which theyare attached form a double bond; each R^(36′) is independently selectedfrom hydrogen, halogen and C₁-C₄ alkyl; R^(37′) and R^(38′) are selectedindependently of each other from the group consisting of hydrogen,halogen, cyano, C₁-C₄ alkyl and C₁-C₄ haloalkyl; R^(39′), R^(40′),R^(41′), R^(42′), R^(43′) and R^(44′) are selected independently of eachother from the group consisting of hydrogen, halogen, hydroxy, cyano,C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄alkylthio; R^(45′), R^(46′), R^(47′), R^(48′) and R^(49′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆ alkoxy, C₁-C₆haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆ alkynyloxy,C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆alkylsulfonyl and C₁-C₆ haloalkylsulfonyl; R^(50′) is selected from thegroup consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl;R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected,independently of each other, from the group consisting of hydrogen,fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkoxy and C₁-C₄alkylthio; R^(57′), R^(58′), R^(59′) and R^(60′) are selected,independently of each other, from the group consisting of hydrogen,halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂,C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₂-C₆ alkoxy, C₂-C₆haloalkoxy, phenyl, C₃-C₆ alkenyloxy, C₃-C₆ haloalkenyloxy, C₃-C₆alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆ halocycloalkoxy, benzyloxy, C₁-C₆alkylthio, C₁-C₆ haloalkylthio, C₁-C₆ alkylsulfinyl, C₁-C₆haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆ haloalkylsulfonyl;provided that at least one of R^(57′), R^(58′), R^(59′) and R^(60′) isnot hydrogen; R^(61′) and R^(62′) are selected independently of eachother from the group consisting of hydrogen, fluorine, cyano, C₁-C₄alkyl and C₁-C₄ haloalkyl; R^(63′), R^(64′), R^(65′), R^(66′), R^(67′)and R^(68′) are selected independently of each other from the groupconsisting of hydrogen, halogen, hydroxy, cyano, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy and C₁-C₄ alkylthio; R^(69′)is selected from hydrogen, C₁-C₄ alkyl, C₃-C₄ alkenyl and C₁-C₄alkylcarboxy; n is 0 or 1; p and q are independently selected from 0 and1; r, s and t are independently selected from 0 and
 1. 4. A fungicidalcomposition according to claim 1, wherein component A) is a compound offormula (I) wherein R₁ and R₂ are each C₁-C₄ alkyl; R₃ representshydrogen, halogen, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄ alkenyl,C₂-C₄ alkynyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl, C₁-C₄ alkylthio, C₁-C₄alkylsulfinyl or C₁-C₄ alkylsulfonyl; R₄ is selected from methyl, ethyl,methoxy, fluorine and chlorine; R₆ is hydrogen; R₇ is hydrogen or C₁-C₄alkyl.
 5. A fungicidal composition according to claim 1, whereincomponent A) is a compound of formula (I) wherein R₁ and R₂ are eachindependently selected from methyl, ethyl and isopropyl; R₃ representshydrogen, halogen, C₁-C₄ alkyl, C₁-C₄ haloalkyl, cyclopropyl, ethynyl orC₁-C₄ alkoxy; R₄ is selected from methyl, methoxy, fluorine andchlorine; R₆ is hydrogen; R₇ is hydrogen.
 6. A fungicidal compositionaccording to claim 1, wherein component A) is a compound of formula (I)wherein R₁ is methyl; R₂ is ethyl; R₃ is selected from hydrogen,bromine, iodine, methyl, CHF₂, cyclopropyl, ethynyl and methoxy; R₄ ismethyl; R₆ is hydrogen; R₇ is hydrogen.
 7. A fungicidal compositionaccording to claim 3, wherein component A) is a compound of formula (I)wherein R₅ is selected from G¹, G², G⁵, G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹²,G¹⁴, G¹⁵ and G¹⁶.
 8. A fungicidal composition according to claim 3,wherein component A) is a compound of formula (I) wherein R₅ is selectedfrom G², G⁵, G⁶-G⁷, G⁸, G⁹, G¹⁰-G¹¹, G¹⁴ and G¹⁶.
 9. A fungicidalcomposition according to claim 3, wherein component A) is a compound offormula (I) wherein R₅ is selected from G², G⁵, G⁸ and G¹⁰-G¹¹.
 10. Afungicidal composition according to claim 3, wherein component A) is acompound of formula (I) wherein G¹ is a C₉-C₁₀ fused bicyclic ringsystem which may be saturated or comprise one carbon-carbon double bondand is optionally substituted by one or more groups independentlyselected from C₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl; G²is C₃-C₆ cycloalkenyl, which is optionally substituted by one or moregroups independently selected from halogen, ethyl, n-propyl, iso-propyl,n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio; G³ is phenyl, which is optionally substituted by one ormore groups independently selected from hydroxyl, C₁-C₄ alkyl, C₁-C₄fluoroalkyl, C₁-C₄ alkoxy and halogen; G⁴ is C₅-C₆ cycloalkyl which isoptionally substituted by one or more groups independently selected fromhydroxyl, C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy,halogen and cyano, wherein the alkyl groups are optionally substitutedby one or more halogen; G⁵ is C₃-C₇ cycloalkyl, which is substituted byone or more groups independently selected from ethyl, n-propyl,iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl,—CH(CH₃)—CH₂—CH₂—CH₃, —CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃,—CH₂—CH₂—CH(CH₃)₂, —CH(CH₃)—CH(CH₃)₂, C₂-C₆ haloalkyl, C₁-C₆ alkoxy,C₃-C₄-alkenyloxy, phenoxy and C₁-C₆ alkylthio; G⁶ is phenyl, which mustbe substituted by at least one fluorine and is optionally furthersubstituted by one or more groups independently selected from halogen,CN, NO₂, OH, SH, CHO, C(═O)NH₂, C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂,C(═S)NH(CH₃), C(═S)N(CH₃)₂, SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl,C₁-C₆ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl,C₂-C₆ alkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆alkynyloxy, C₁-C₆ alkylthio, C₁-C₆ alkylsulfinyl and C₁-C₆alkylsulfonyl; G¹⁰ is phenyl, which is optionally substituted by one ormore groups independently selected from halogen, CN, OH, SH, CHO,methyl, ethyl, n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃,CF₂—CF₃, cyclopropyl, CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃),CH═C(CH₃)₂, C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy,iso-propyloxy, phenyl, OCHF₂, OCH₂—C≡CH, OCH(CH₃)—C≡CH, SCH₃, SCH₂CH₃,S(═O)CH₃, S(═O)CH₂CH₃, S(═O)₂CH₃ and S(═O)₂CH₂CH₃; G¹¹ is methylenesubstituted by at least one group independently selected from C₁-C₄alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy and C₁-C₄ haloalkoxy; G¹³ is aC₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or N atoms, whereinthere are no adjacent O atoms, which is optionally substituted by one ormore groups independently selected from halogen, C₁-C₆ alkyl, C₁-C₆haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and ═O; G¹⁷ is a five- tosix-membered monocyclic heteroaromatic ring system which can contain 1to 4 members selected from the group consisting of N, N(R^(69′)), O andS, it not being possible for each ring system to contain —O—O—, —S—S—and —O—S— fragments, and it being possible for the five- to six-memberedring system to be itself mono- or polysubstituted by groups selectedfrom the group consisting of halogen, CN, NO₂, OH, SH, CHO, C(═O)NH₂,C(═O)NH(CH₃), C(═O)N(CH₃)₂, C(═S)NH₂, C(═S)NH(CH₃), C(═S)N(CH₃)₂,SO₂NH₂, SO₂NH(CH₃), SO₂N(CH₃)₂, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₃-C₆cycloalkyl, C₂-C₆ alkenyl, C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆haloalkynyl, C₁-C₆ alkoxy, C₁-C₆ haloalkoxy, C₃-C₆ alkenyloxy, C₃-C₆haloalkenyloxy, C₃-C₆ alkynyloxy, C₃-C₆ cycloalkoxy, C₃-C₆halocycloalkoxy, C₁-C₆ alkylthio, C₁-C₆ haloalkylthio, C₁-C₆alkylsulfinyl, C₁-C₆ haloalkylsulfinyl, C₁-C₆ alkylsulfonyl and C₁-C₆haloalkylsulfonyl; R^(1′) is selected from the group consisting ofhydrogen, fluorine, C₁-C₄ alkyl and C₁-C₄ fluoroalkyl; R^(2′), R^(3′),R^(4′) and R^(5′) are selected, independently of each other, from thegroup consisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl,C₁-C₄ alkoxy and C₁-C₄ alkylthio; R^(11′), R^(12′), R^(13′) and R^(14′)are selected, independently of each other, from the group consisting ofhydrogen, cyano, halogen, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy andC₁-C₆ alkylthio; R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′),R^(21′) and R^(22′) are independently selected from the group consistingof hydrogen, halogen, methyl, ethyl, isopropyl, CH₂F, CHF₂, CF₃,CHF—CH₃, CF₂—CH₃ and CF₂CF₃; R^(23′), R^(24′) and R^(25′) areindependently selected from the group consisting of hydrogen, halogen,cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₃-C₆ cycloalkyl,C₃-C₆ halocycloalkyl and C₁-C₄ alkylthio; R^(26′) is N—OH, N—O— C₁-C₄alkyl, N—O— C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl, N—O— C₁-C₄ haloalkyl,N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O orC(R^(36′))₂; R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′),R^(33′), R^(34′) and R^(35′) are each independently selected from thegroup consisting of hydrogen, hydroxyl, C₁-C₄ alkyl, C₁-C₄ alkoxy andhalogen; or R^(28′) and R^(29′) together with the two carbon atoms towhich they are attached form a double bond; each R^(36′) isindependently selected from hydrogen, halogen and C₁-C₄ alkyl; R^(37′),R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) areselected independently of each other from a group consisting ofhydrogen, halogen, methyl, ethyl, isopropyl, monofluoromethyl,polyfluoromethyl, monofluoroethyl, and polyfluoroethyl; R^(45′),R^(46′), R^(47′), R^(48′) and R^(49′) are independently selected fromthe group consisting of hydrogen, fluorine, chlorine, bromine, iodine,methyl, ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃,CHF₂, CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, ethoxy, difluoromethoxy,trifluoromethoxy, methlythio, methylsulfinyl and methylsulfonyl; R^(50′)is selected from the group consisting of hydrogen, fluorine, C₁-C₄alkyl, C₁-C₄ haloalkyl; R^(51′), R^(52′), R^(53′), R^(54′), R^(55′) andR^(56′) are selected, independently of each other, from the groupconsisting of hydrogen, fluorine, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₂-C₄alkoxy and C₁-C₄ haloalkoxy; R^(57′), R^(58′), R^(59′) and R^(60′) areselected, independently of each other, from the group consisting ofhydrogen, cyano, halogen, C₁-C₆ alkyl and C₁-C₆ haloalkyl; provided thatat least one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen;R^(61′) and R^(62′) are selected independently of each other from thegroup consisting of hydrogen, fluorine, cyano, C₁-C₄ alkyl and C₁-C₄haloalkyl; R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) areselected independently of each other from the group consisting ofhydrogen, fluorine, cyano, C₁-C₄ alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxyand C₁-C₄ haloalkoxy; R^(69′) is selected from hydrogen, C₁-C₄ alkyl andC₁-C₄ alkylcarboxy; n is 0 or 1; p and q are independently selected from0 and 1; r and s are 0 and t is 1 or
 0. 11. A fungicidal compositionaccording to claim 3, wherein component A) is a compound of formula (I)wherein G¹ is a saturated C₁₀ fused bicyclic ring system which isoptionally substituted by one or more groups independently selected fromC₁-C₄ alkyl, fluorine, methoxy and C₁-C₄ fluoroalkyl; G² is a C₅-C₆cycloalkenyl group optionally substituted by one or more fluorine atoms;G³ is phenyl, which is optionally substituted by one or more groupsindependently selected from hydroxyl, C₁-C₄ alkyl, CHF₂, CF₃, C₁-C₄alkoxy and halogen; G⁴ is C₅-C₆ cycloalkyl which is optionallysubstituted by one or more groups independently selected from hydroxyl,C₁-C₄ alkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl, C₁-C₄ alkoxy and halogen; G⁵is C₅-C₆ cycloalkyl, which is substituted by one or more groupsindependently selected from ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂,—CH(CH₃)—CH(CH₃)₂ and C₂-C₆ haloalkyl; G⁶ is phenyl, which must besubstituted by at least one fluorine and is optionally furthersubstituted by one or more groups independently selected from halogen,CN, C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄ alkoxy; G⁷ is methylene; G¹⁰is phenyl, which is optionally substituted by one or more groupsindependently selected from hydrogen, halogen, CN, OH, methyl, ethyl,n-propyl, iso-propyl, CH₂F, CHF₂, CF₃, CHF—CH₃, CF₂—CH₃, CF₂—CF₃,CH═CH₂, C(CH₃)═CH₂, CH═CH(CH₃), C(CH₃)═CH(CH₃), CH═C(CH₃)₂,C(CH₃)═C(CH₃)₂, CH═CF₂, CH═CCl₂, C≡CH, methoxy, ethoxy, iso-propyloxy,phenyl and OCHF₂; G¹¹ is methylene substituted by at least one groupindependently selected from C₁-C₄ alkyl, C₁-C₄ haloalkyl and C₁-C₄alkoxy; G¹³ is a C₈-C₁₁ spirobicyclic system containing 0, 1 or 2 O or Natoms, wherein there are no adjacent O atoms, which is optionallysubstituted by one or more groups independently selected from halogen,C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆ alkoxy, C₁-C₆ alkylthio and ═O; G¹⁷is a five- to six-membered monocyclic heteroaromatic ring system whichcan contain 1 to 4 members selected from the group consisting of N,N(R^(69′)), O and S it not being possible for each ring system tocontain —O—O—, —S—S— and —O—S— fragments, and it being possible for thefive- to six-membered ring system to be itself mono- or polysubstitutedby groups selected from the group consisting of halogen, CN, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl orbenzyl, wherein the phenyl or benzyl are optionally substituted byhalogen, CN, C₁-C₄ alkyl or C₁-C₄ haloalkyl; R^(1′) is selected from thegroup consisting of hydrogen, fluorine, methyl, CH₂F and CF₃; R^(2′),R^(3′), R^(4′) and R^(5′) are selected, independently of each other,from the group consisting of hydrogen, fluorine, methyl, CH₂F, CF₃ andmethoxy; R^(11′), R^(12′), R^(13′) and R^(14′) are selected,independently of each other, from the group consisting of hydrogen,halogen, cyano, C₁-C₄ alkyl, CHF₂, CF₃ and C₁-C₄ alkoxy; R^(15′),R^(16′), R^(17′), R^(18′), R^(19′), R^(20′), R^(21′) and R^(22′) areeach independently selected from hydrogen, fluorine, methyl, ethyl,CH₂F, CHF₂, CF₃ and isopropyl; R^(23′), R^(24′) and R^(25′) areindependently selected from the group consisting of hydrogen, methyl,fluorine, chlorine, bromine, ethyl, CH₂F, CHF₂, CF₃ and isopropyl;R^(26′) is selected from the group consisting of N—OH, N—O— C₁-C₄ alkyl,N—O— C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl, N—O— C₁-C₄ haloalkyl, N—O—C₂-C₄haloalkenyl, N—O-benzyl, N—O-phenyl, N—O-halophenyl, O, and C(R^(36′));R^(27′), R^(28′), R^(29′), R^(30′), R^(31′), R^(32′), R^(33′), R^(34′)and R^(35′) are each independently selected from the group consisting ofhydrogen, C₁-C₄ alkyl and halogen; or R^(27′) and R^(28′) together withthe two carbon atoms to which they are attached form a double bond; eachR^(36′) is independently selected from hydrogen, halogen and C₁-C₄alkyl; R^(37′), R^(38′), R^(39′), R^(40′), R^(41′), R^(42′), R^(43′) andR^(44′) are independently selected from the group consisting ofhydrogen, fluorine, methyl and trifluoromethyl; R^(45′), R^(46′),R^(47′), R^(48′) and R^(49′) are independently selected from the groupconsisting of hydrogen, fluorine, chlorine, bromine, iodine, methyl,ethyl, isopropyl, cyclopropyl, C≡CH, CH═CH₂, C(CH₃)═CH₂, CF₃, CHF₂,CH₂F, —CHF—CH₃, —CF₂—CH₃, methoxy, difluoromethoxy, trifluoromethoxy,ethoxy, methlythio, methylsulfinyl and methylsulfonyl; R^(50′), R^(51′),R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are selected,independently of each other, from the group consisting of hydrogen,fluorine, methyl, CH₂F and CF₃; R^(57′), R^(58′), R^(59′) and R^(60′)are selected, independently of each other, from the group consisting ofhydrogen, halogen, cyano, C₁-C₄ alkyl, CHF₂ and CF₃; provided that atleast one of R^(57′), R^(58′), R^(59′) and R^(60′) is not hydrogen;R^(61′) and R^(62′) are selected independently of each other from thegroup consisting of hydrogen, fluorine, methyl, ethyl, CHF₂ and CF₃;R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′) and R^(68′) areselected independently of each other from the group consisting ofhydrogen, fluoro, methyl, ethyl, methoxy, difluoromethoxy,trifluoromethoxy, CHF₂ and CF₃; R^(69′) is selected from hydrogen andC₁-C₄ alkyl; n is 0 or 1; p and q are independently selected from 0 and1; r and s are 0 and t is 1 or
 0. 12. A fungicidal composition accordingto claim 3, wherein component A) is a compound of formula (I) wherein G¹is a saturated C₁₀ fused bicyclic ring system; G² is a C₅-C₆cycloalkenyl group; G³ is phenyl; G⁴ is cyclohexyl or cyclopentyl; G⁵ isC₆ cycloalkyl, which is optionally substituted by one or more groupsindependently selected from ethyl, n-propyl, iso-propyl, n-butyl,iso-butyl, sec-butyl, tert-butyl, n-pentyl, —CH(CH₃)—CH₂—CH₂—CH₃,—CH—CH(CH₃)—CH₂—CH₃, —CH₂—CH₂—CH(CH₃)—CH₃, —CH₂—CH₂—CH(CH₃)₂ and—CH(CH₃)—CH(CH₃)₂; G⁶ is phenyl, which must be substituted by at leastone fluorine and is optionally further substituted by one or moremethyl, bromine, iodine or chlorine; G⁷ is methylene; G¹⁰ is phenyl,which is optionally substituted by one or more groups independentlyselected from halogen, CN, methyl, ethyl, n-propyl, iso-propyl, ethenyl,methoxy, ethoxy, iso-propyloxy, phenyl, CHF₂, CF₃, CHF—CH₃ and OCHF₂;G¹¹ is methylene substituted by at least one group independentlyselected from methyl, CF₃ and ethyl; G¹³ is a C₈-C₁₁ spirobicyclicsystem containing 0, 1 or 2 O or N atoms, wherein there are no adjacentO atoms, which is optionally substituted by one or more groupsindependently selected from halogen, C₁-C₄ alkyl, C₁-C₄ alkoxy and ═O;G¹⁷ is a five- to six-membered monocyclic heteroaromatic ring systemwhich can contain 1 or 2 members selected from the group consisting ofN, O and S, it not being possible for each ring system to contain —O—O—,—S—S— and —O—S— fragments, and it being possible for the five- tosix-membered ring system to be itself mono- or polysubstituted by groupsselected from the group consisting of halogen, CN, C₁-C₄ alkyl, C₁-C₄haloalkyl, C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, phenyl or fluorophenyl;R^(1′), R^(2′), R^(3′), R^(4′) and R^(5′) are each hydrogen; R^(11′),R^(12′), R^(13′) and R^(14′) are selected, independently of each other,from the group consisting of hydrogen, halogen, cyano, C₁-C₄ alkyl andC₁-C₄ alkoxy; R^(15′), R^(16′), R^(17′), R^(18′), R^(19′), R^(20′),R^(21′), R^(22′), R^(23′), R^(24′) and R^(25′) are each independentlyselected from hydrogen, methyl, ethyl and isopropyl; R^(26′) is N—OH,N—O— C₁-C₄ alkyl, N—O— C₂-C₄ alkenyl, N—O—C₂-C₄ alkynyl, N—O— C₁-C₄haloalkyl, N—O—C₂-C₄ haloalkenyl, N—O-benzyl, N—O-phenyl,N—O-halophenyl, O and C(R^(36′)); R^(27′), R^(28′), R^(29′), R^(30′),R^(31′), R^(32′), R^(33′), R^(34′) and R³⁵ are each hydrogen or methyl;or R^(27′) and R^(28′) together with the two carbon atoms to which theyare attached form a double bond; each R^(36′) is independently selectedfrom hydrogen, halogen and C₁-C₄ alkyl; R^(37′), R^(38′), R^(39′),R^(40′), R^(41′), R^(42′), R^(43′) and R^(44′) are hydrogen; R^(45′),R^(46′), R^(47′), R^(48′) and R^(49′) are independently selected fromthe group consisting of hydrogen, fluorine, chlorine, methyl, CF₃, CHF₂,CH₂F, methoxy, difluoromethoxy and trifluoromethoxy; R^(53′), R^(51′),R^(52′), R^(53′), R^(54′), R^(55′) and R^(56′) are each hydrogen;R^(57′), R^(58′), R^(59′) and R^(60′) are selected, independently ofeach other, from the group consisting of hydrogen and halogen; providedthat at least one of R^(57′), R^(58′), R^(59′) and R^(60′) is nothydrogen; R^(61′), R^(62′), R^(63′), R^(64′), R^(65′), R^(66′), R^(67′)and R^(68′) are hydrogen; R^(69′) is hydrogen; n is 0 or 1; p and q areindependently selected from 0 and 1; r, s and t are each
 0. 13. Acompound according to formula (IV)

wherein R₁₀₀ is halogen, SH, C₁-C₄ alkylthio, C₁-C₄-alkysulfinyl, C₁-C₄alkylsulfonyl; R₁ and R₂ are each independently selected from hydrogen,C₁-C₄ alkyl, C₃-C₄ alkenyl, C₃-C₄ alkynyl, (R₁₀)carbonyl and(R₁₀)oxycarbonyl; or R₁ and R₂ together with the nitrogen atom to whichthe are attached form a 5- or 6 membered cyclic group which may besaturated or unsaturated and may contain a further heteroatom selectedfrom S or O; R³ represents hydrogen, halogen, cyano, nitro, mercapto,hydroxy, —C(═S)NH₂, —SF₅, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₂-C₆ alkenyl,C₂-C₆ haloalkenyl, C₂-C₆ alkynyl, C₂-C₆ haloalkynyl, C₁-C₆alkoxy, C₁-C₆haloalkoxy, C₃-C₆cycloalkyl amino, C₁-C₂ alkylamino,di(C₁-C₆alkyl)amino, a 5-membered heterocycle containing 1-4 nitrogenatoms, piperidino, morpholino, thiomorpholino, formyl, hydroxycarbonyl,C₂-C₇ alkoxycarbonyl, C₂-C₇ haloalkoxycarbonyl, C₄-C₇alkenyloxycarbonyl, C₄-C₇ haloalkenyloxycarbonyl, C₂-C₇ alkylcarbonyl,C₂-C₇ haloalkylcarbonyl, C₁-C₆alkylthio, C₁-C₆alkylsulfinyl,C₁-C₆alkylsulfonyl, C₁-C₆ haloalkylthio, C₁-C₆ haloalkylsulfinyl, C₁-C₆haloalkylsulfonyl, C₁-C₆ hydroxyalkyl, phenyl or benzyl wherein thephenyl and benzyl are optionally substituted by one or more groupsindependently selected from the group consisting of halogen, cyano,hydroxy, mercapto, amino, C₁-C₆ alkyl, C₁-C₆ haloalkyl, C₁-C₆alkoxy,C₁-C₆ haloalkoxy, C₁-C₆alkylthio, C₁-C₆alkylsulfinyl andC₁-C₆alkylsulfonyl; R₄ represents hydrogen, halogen, cyano, amino, C₁-C₄alkyl, C₁-C₄ haloalkyl, C₃-C₆ cycloalkyl, C₂-C₄ alkenyl, C₂-C₄ alkynyl,C₁-C₄ alkoxy, C₁-C₄ haloalkoxy, C₁-C₄ alkylthio, C₁-C₄ alkylsulfinyl,C₁-C₄ alkylsulfonyl, methylamino or dimethylamino; R₆ is selected fromhydrogen and SH; and R₇ is hydrogen, halogen or C₁-C₄ alkyl.
 14. Amethod of controlling phytopathogenic diseases on useful plants or onpropagation material thereof, which comprises applying to the usefulplants, the locus thereof or propagation material thereof a combinationof components A) and B) in a synergistically effective amount accordingto claim 1 together with an inert carrier, and optionally an adjuvant.15. A fungicidal composition, comprising a combination of components A)and B) according to claim 1 together with an inert carrier, andoptionally an adjuvant, wherein the weight ratio of A) to B) is between100:1 and 1:6000.
 16. A method of protecting natural substances of plantorigin, which have been taken from their natural life cycle, and/ortheir processed forms, which comprises applying to said naturalsubstances of plant and/or animal origin or their processed forms acombination of components A) and B) according to claim 1 in asynergistically effective amount.